FCC ID Z7AB7000

Z7A-B7000, Z7A B7000, Z7AB7000, Z7AB7OOO

Stryker Medical Communication Module B7000

An FCC ID is the product ID assigned by the FCC to identify wireless products in the market. The FCC chooses 3 or 5 character "Grantee" codes to identify the business that created the product. For example, the grantee code for FCC ID: Z7AB7000 is Z7A. The remaining characters of the FCC ID, B7000, are often associated with the product model, but they can be random. These letters are chosen by the applicant. In addition to the application, the FCC also publishes internal images, external images, user manuals, and test results for wireless devices. They can be under the "exhibits" tab below.

Purchase on Amazon: Communication Module

App # Purpose Date Unique ID
1 Change in Identification 2025-03-14 q7P+pA7WCHikXgmz4JVioA==
2 Change in Identification 2025-03-14 WQ5WWa8OtjkIFYx21e2u3w==
3 Change in Identification 2025-03-14 QTL5HQdMy93X2wkqlTREEQ==
4 Change in Identification 2025-03-14 H8NSXcqI9zkKotaNd4CpQg==
5 Change in Identification 2025-03-14 /zCPb5YhdwL/fS3R3wzJ2g==

Operating Frequencies

Frequency RangePower OutputRule PartsGrant Notes App #
2.402-2.48 GHz Bluetooth11 mW15CCC, MO 3.1
2.402-2.48 GHz Bluetooth12 mW15CCC, MO 4.1
2.412-2.462 GHz 2.4 GHz WiFi497 mW15CCC, MO 4.2
5.18-5.24 GHz 5 GHz WiFi63 mW15ECC, MO 1.1
5.26-5.32 GHz 5 GHz WiFi DFS62 mW15ECC, MO 1.2
5.5-5.72 GHz 5 GHz WiFi61 mW15ECC, MO 1.3
5.745-5.825 GHz 5 GHz WiFi63 mW15ECC, MO 1.4
5.955-7.095 GHz24 mW15ECC, MO 2.1
5.955-7.095 GHz95 mW15ECC, MO 5.1

Application Forms

Application for Equipment Authorization FCC Form 731 TCB Version


Applicant Information
Applicant's complete, legal business name: Stryker Medical
FCC Registration Number (FRN): 0017033432
Alphanumeric FCC ID: Z7AB7000
Unique Application Identifier: q7P+pA7WCHikXgmz4JVioA==
Line one: 3800 East Centre Ave
City: Portage
State: Michigan
Country: United States
Zip Code: 49002

TCB Information
TCB Application Email Address: tcb_admin@intertek.com
TCB Scope: A4: UNII devices & low power transmitters using spread spectrum techniques

FCC ID
Grantee Code: Z7A
Product Code: B7000

Person at the applicant's address to receive grant or for contact
Name: Divya Murali
Title: Director, Global Regulatory Affairs
Telephone Number: 2695678254 Extension:
Fax Number: 2693851062
Email: divya.murali@stryker.com

Technical Contact
Firm Name:
Stryker Medical
First Name: Lionel
Last Name: Gabrillo
Line 1:
3030 Orchard Pkwy
City: San Jose
State: California
Country:
United States
Zip Code: 95134
Telephone Number:
408-833-6543

Extension:
E-Mail:

Non Technical Contact
Firm Name: Stryker Medical
First Name: Roc
Last Name: Jiang
Line 1: 3030 Orchard Pkwy
City: San Jose
State: California
Country: United States
Zip Code: 95134
Telephone Number: 510-240-0517 Extension:
E-Mail: Roc.jiang@stryker.com

Long-Term Confidentiality
Does this application include a request for confidentiality for any portion(s) of the data contained in this application pursuant to 47 CFR § 0.459 of the Commission Rules?:   Yes

Short-Term Confidentiality
Does short-term confidentiality apply to this application?:   No
If so, specify the short-term confidentiality release date (MM/DD/YYYY format):  
Note: If no date is supplied, the release date will be set to 45 calendar days past the date of grant.

Software Defined/Cognitive Radio
Is this application for software defined/cognitive radio authorization?   Yes

Equipment Class
Equipment Class:   NII - Unlicensed National Information Infrastructure TX
Description of product as it is marketed: (NOTE: This text will appear below the equipment class on the grant): Communication Module

Related OET KnowledgeDataBase Inquiry
Is there a KDB inquiry associated with this application?  Yes

Modular Equipment
Modular Type:  Single Modular Approval

Application Purpose
Application is for:   Change in identification of presently authorized equipment. Original FCC ID: VPYLBEE5XV2EA Grant Date: 08/19/2023

Composite/Related Equipment
Is the equipment in this application a composite device subject to an additional equipment authorization?   Yes
Is the equipment in this application part of a system that operates with, or is marketed with, another device that requires an equipment authorization?   No


Test Firm Information
Name of test firm and contact person on file with the FCC:
Firm Name:   SGS Taiwan Ltd. Central RF Lab
First Name:   Ryan
Last Name:   WANG
Telephone Number: 886222993279 Extension: 1473
E-mail:  ryan-ec.wang@sgs.com

Grant Comments
Enter any text that you would like to appear at the bottom of the Grant of Equipment Authorization:
Limited Module Approval Software Defined Radio. Output Power listed is the maximum conducted output power. This device must be installed and operated so as to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi-transmitter product procedures, or as evaluated in this filing. This device supports 20, 40 , and 80 MHz modes. Restricted to indoor use only in 6GHz band. Operation in the 5250-5350 MHz and 5470 - 5725MHz limited to Client only operation.
Set the grant of this application to be deferred to a specified date:
No

Equipment Authorization Waiver
Is there an equipment authorization waiver associated with this application?  No
If there is an equipment authorization waiver associated with this application, has the associated waiver been approved and all information uploaded?:  No

WILLFUL FALSE STATEMENTS MADE ON THIS FORM ARE PUNISHABLE BY FINE AND IMPRISONMENT (U.S. CODE, TITLE 18, SECTION 1001), AND/OR REVOCATION OF ANY STATION LICENSE OR CONSTRUCTION PERMIT (U.S. CODE, TITLE 47, SECTION 312(a)(1)), AND/OR FORFEITURE (U.S. CODE, TITLE 47, SECTION 503).

SECTION 5301 (ANTI-DRUG ABUSE) CERTIFICATION:
The applicant must certify that neither the applicant nor any party to the application is subject to a denial of Federal benefits, that include FCC benefits, pursuant to Section 5301 of the Anti-Drug Abuse Act of 1988, 21 U.S.C. § 862 because of a conviction for possession or distribution of a controlled substance. See 47 CFR 1.2002(b) for the definition of a "party" for these purposes.

Does the applicant or authorized agent so certify?  Yes

Applicant/Agent Certification:

I certify that I am authorized to sign this application. All of the statements herein and the exhibits attached hereto, are true and correct to the best of my knowledge and belief. In accepting a Grant of Equipment Authorization as a result of the representations made in this application, the applicant is responsible for (1) labeling the equipment with the exact FCC ID specified in this application, (2) compliance statement labeling pursuant to the applicable rules, and (3) compliance of the equipment with the applicable technical rules. If the applicant is not the actual manufacturer of the equipment, appropriate arrangements have been made with the manufacturer to ensure that production units of this equipment will continue to comply with the FCC's technical requirements.

Authorizing an agent to sign this application, is done solely at the applicant's discretion; however, the applicant remains responsible for all statements in this application.

If an agent has signed this application on behalf of the applicant, a written letter of authorization which includes information to enable the agent to respond to the above section 5301 (Anti-Drug Abuse) Certification statement has been provided by the applicant. It is understood that the letter of authorization must be submitted to the FCC upon request, and that the FCC reserves the right to contact the applicant directly at any time.

Signature of Authorized Person Filing:  Dita Paul
Title of authorized signature:  Director RAQA Digital Health

Complete items below if agent signs the application:

Firm Name:  Stryker Medical
Name:  Dita Dita Dita
Line 1:  Dita
Line 2:  Dita
P.O. Box:  Dita
City:  Dita
State:  Dita
Country:  Dita
Zip Code:  Dita

Application for Equipment Authorization FCC Form 731 TCB Version


Applicant Information
Applicant's complete, legal business name: Stryker Medical
FCC Registration Number (FRN): 0017033432
Alphanumeric FCC ID: Z7AB7000
Unique Application Identifier: WQ5WWa8OtjkIFYx21e2u3w==
Line one: 3800 East Centre Ave
City: Portage
State: Michigan
Country: United States
Zip Code: 49002

TCB Information
TCB Application Email Address: tcb_admin@intertek.com
TCB Scope: A4: UNII devices & low power transmitters using spread spectrum techniques

FCC ID
Grantee Code: Z7A
Product Code: B7000

Person at the applicant's address to receive grant or for contact
Name: Divya Murali
Title: Director, Global Regulatory Affairs
Telephone Number: 2695678254 Extension:
Fax Number: 2693851062
Email: divya.murali@stryker.com

Technical Contact
Firm Name:
Stryker Medical
First Name: Lionel
Last Name: Gabrillo
Line 1:
3030 Orchard Pkwy
City: San Jose
State: California
Country:
United States
Zip Code: 95134
Telephone Number:
408-833-6543

Extension:
E-Mail:

Non Technical Contact
Firm Name: Stryker Medical
First Name: Roc
Last Name: Jiang
Line 1: 3030 Orchard Pkwy
City: San Jose
State: California
Country: United States
Zip Code: 95134
Telephone Number: 510-240-0517 Extension:
E-Mail: Roc.jiang@stryker.com

Long-Term Confidentiality
Does this application include a request for confidentiality for any portion(s) of the data contained in this application pursuant to 47 CFR § 0.459 of the Commission Rules?:   No

Short-Term Confidentiality
Does short-term confidentiality apply to this application?:   No
If so, specify the short-term confidentiality release date (MM/DD/YYYY format):  
Note: If no date is supplied, the release date will be set to 45 calendar days past the date of grant.

Software Defined/Cognitive Radio
Is this application for software defined/cognitive radio authorization?   Yes

Equipment Class
Equipment Class:   6XD - 15E 6 GHz Low Power Indoor Client
Description of product as it is marketed: (NOTE: This text will appear below the equipment class on the grant): Communication Module

Related OET KnowledgeDataBase Inquiry
Is there a KDB inquiry associated with this application?  Yes

Modular Equipment
Modular Type:  Single Modular Approval

Application Purpose
Application is for:   Change in identification of presently authorized equipment. Original FCC ID: VPYLBEE5XV2EA Grant Date: 08/19/2023

Composite/Related Equipment
Is the equipment in this application a composite device subject to an additional equipment authorization?   Yes
Is the equipment in this application part of a system that operates with, or is marketed with, another device that requires an equipment authorization?   No


Test Firm Information
Name of test firm and contact person on file with the FCC:
Firm Name:   SGS Taiwan Ltd. Central RF Lab
First Name:   Ryan
Last Name:   WANG
Telephone Number: 886222993279 Extension: 1473
E-mail:  ryan-ec.wang@sgs.com

Grant Comments
Enter any text that you would like to appear at the bottom of the Grant of Equipment Authorization:
Limited Module Approval Software Defined Radio. Output Power listed is the maximum conducted output power. This device must be installed and operated so as to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi-transmitter product procedures, or as evaluated in this filing. This device supports 20, 40 , 80 and 160 MHz modes. Restricted to indoor use only in 6GHz band
Set the grant of this application to be deferred to a specified date:
No

Equipment Authorization Waiver
Is there an equipment authorization waiver associated with this application?  No
If there is an equipment authorization waiver associated with this application, has the associated waiver been approved and all information uploaded?:  No

WILLFUL FALSE STATEMENTS MADE ON THIS FORM ARE PUNISHABLE BY FINE AND IMPRISONMENT (U.S. CODE, TITLE 18, SECTION 1001), AND/OR REVOCATION OF ANY STATION LICENSE OR CONSTRUCTION PERMIT (U.S. CODE, TITLE 47, SECTION 312(a)(1)), AND/OR FORFEITURE (U.S. CODE, TITLE 47, SECTION 503).

SECTION 5301 (ANTI-DRUG ABUSE) CERTIFICATION:
The applicant must certify that neither the applicant nor any party to the application is subject to a denial of Federal benefits, that include FCC benefits, pursuant to Section 5301 of the Anti-Drug Abuse Act of 1988, 21 U.S.C. § 862 because of a conviction for possession or distribution of a controlled substance. See 47 CFR 1.2002(b) for the definition of a "party" for these purposes.

Does the applicant or authorized agent so certify?  Yes

Applicant/Agent Certification:

I certify that I am authorized to sign this application. All of the statements herein and the exhibits attached hereto, are true and correct to the best of my knowledge and belief. In accepting a Grant of Equipment Authorization as a result of the representations made in this application, the applicant is responsible for (1) labeling the equipment with the exact FCC ID specified in this application, (2) compliance statement labeling pursuant to the applicable rules, and (3) compliance of the equipment with the applicable technical rules. If the applicant is not the actual manufacturer of the equipment, appropriate arrangements have been made with the manufacturer to ensure that production units of this equipment will continue to comply with the FCC's technical requirements.

Authorizing an agent to sign this application, is done solely at the applicant's discretion; however, the applicant remains responsible for all statements in this application.

If an agent has signed this application on behalf of the applicant, a written letter of authorization which includes information to enable the agent to respond to the above section 5301 (Anti-Drug Abuse) Certification statement has been provided by the applicant. It is understood that the letter of authorization must be submitted to the FCC upon request, and that the FCC reserves the right to contact the applicant directly at any time.

Signature of Authorized Person Filing:  Dita Paul
Title of authorized signature:  Director RAQA Digital Health

Complete items below if agent signs the application:

Firm Name:  Stryker Medical
Name:  Dita Dita Dita
Line 1:  Dita
Line 2:  Dita
P.O. Box:  Dita
City:  Dita
State:  Dita
Country:  Dita
Zip Code:  Dita

Application for Equipment Authorization FCC Form 731 TCB Version


Applicant Information
Applicant's complete, legal business name: Stryker Medical
FCC Registration Number (FRN): 0017033432
Alphanumeric FCC ID: Z7AB7000
Unique Application Identifier: QTL5HQdMy93X2wkqlTREEQ==
Line one: 3800 East Centre Ave
City: Portage
State: Michigan
Country: United States
Zip Code: 49002

TCB Information
TCB Application Email Address: tcb_admin@intertek.com
TCB Scope: A4: UNII devices & low power transmitters using spread spectrum techniques

FCC ID
Grantee Code: Z7A
Product Code: B7000

Person at the applicant's address to receive grant or for contact
Name: Divya Murali
Title: Director, Global Regulatory Affairs
Telephone Number: 2695678254 Extension:
Fax Number: 2693851062
Email: divya.murali@stryker.com

Technical Contact
Firm Name:
Stryker Medical
First Name: Lionel
Last Name: Gabrillo
Line 1:
3030 Orchard Pkwy
City: San Jose
State: California
Country:
United States
Zip Code: 95134
Telephone Number:
408-833-6543

Extension:
E-Mail:

Non Technical Contact
Firm Name: Stryker Medical
First Name: Roc
Last Name: Jiang
Line 1: 3030 Orchard Pkwy
City: San Jose
State: California
Country: United States
Zip Code: 95134
Telephone Number: 510-240-0517 Extension:
E-Mail: Roc.jiang@stryker.com

Long-Term Confidentiality
Does this application include a request for confidentiality for any portion(s) of the data contained in this application pursuant to 47 CFR § 0.459 of the Commission Rules?:   Yes

Short-Term Confidentiality
Does short-term confidentiality apply to this application?:   No
If so, specify the short-term confidentiality release date (MM/DD/YYYY format):  
Note: If no date is supplied, the release date will be set to 45 calendar days past the date of grant.

Software Defined/Cognitive Radio
Is this application for software defined/cognitive radio authorization?   Yes

Equipment Class
Equipment Class:   DSS - Part 15 Spread Spectrum Transmitter
Description of product as it is marketed: (NOTE: This text will appear below the equipment class on the grant): Communication Module

Related OET KnowledgeDataBase Inquiry
Is there a KDB inquiry associated with this application?  Yes

Modular Equipment
Modular Type:  Single Modular Approval

Application Purpose
Application is for:   Change in identification of presently authorized equipment. Original FCC ID: VPYLBEE5XV2EA Grant Date: 08/19/2023

Composite/Related Equipment
Is the equipment in this application a composite device subject to an additional equipment authorization?   Yes
Is the equipment in this application part of a system that operates with, or is marketed with, another device that requires an equipment authorization?   No


Test Firm Information
Name of test firm and contact person on file with the FCC:
Firm Name:   SGS Taiwan Ltd. Central RF Lab
First Name:   Ryan
Last Name:   WANG
Telephone Number: 886222993279 Extension: 1473
E-mail:  ryan-ec.wang@sgs.com

Grant Comments
Enter any text that you would like to appear at the bottom of the Grant of Equipment Authorization:
Limited Module Approval Software Defined Radio. Output Power listed is the maximum conducted output power. This device must be installed and operated so as to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi-transmitter product procedures, or as evaluated in this filing.
Set the grant of this application to be deferred to a specified date:
No

Equipment Authorization Waiver
Is there an equipment authorization waiver associated with this application?  No
If there is an equipment authorization waiver associated with this application, has the associated waiver been approved and all information uploaded?:  No

WILLFUL FALSE STATEMENTS MADE ON THIS FORM ARE PUNISHABLE BY FINE AND IMPRISONMENT (U.S. CODE, TITLE 18, SECTION 1001), AND/OR REVOCATION OF ANY STATION LICENSE OR CONSTRUCTION PERMIT (U.S. CODE, TITLE 47, SECTION 312(a)(1)), AND/OR FORFEITURE (U.S. CODE, TITLE 47, SECTION 503).

SECTION 5301 (ANTI-DRUG ABUSE) CERTIFICATION:
The applicant must certify that neither the applicant nor any party to the application is subject to a denial of Federal benefits, that include FCC benefits, pursuant to Section 5301 of the Anti-Drug Abuse Act of 1988, 21 U.S.C. § 862 because of a conviction for possession or distribution of a controlled substance. See 47 CFR 1.2002(b) for the definition of a "party" for these purposes.

Does the applicant or authorized agent so certify?  Yes

Applicant/Agent Certification:

I certify that I am authorized to sign this application. All of the statements herein and the exhibits attached hereto, are true and correct to the best of my knowledge and belief. In accepting a Grant of Equipment Authorization as a result of the representations made in this application, the applicant is responsible for (1) labeling the equipment with the exact FCC ID specified in this application, (2) compliance statement labeling pursuant to the applicable rules, and (3) compliance of the equipment with the applicable technical rules. If the applicant is not the actual manufacturer of the equipment, appropriate arrangements have been made with the manufacturer to ensure that production units of this equipment will continue to comply with the FCC's technical requirements.

Authorizing an agent to sign this application, is done solely at the applicant's discretion; however, the applicant remains responsible for all statements in this application.

If an agent has signed this application on behalf of the applicant, a written letter of authorization which includes information to enable the agent to respond to the above section 5301 (Anti-Drug Abuse) Certification statement has been provided by the applicant. It is understood that the letter of authorization must be submitted to the FCC upon request, and that the FCC reserves the right to contact the applicant directly at any time.

Signature of Authorized Person Filing:  Dita Pual
Title of authorized signature:  Director RAQA Digital Health

Complete items below if agent signs the application:

Firm Name:  Stryker Medical
Name:  Dita Dita Dita
Line 1:  Dita
Line 2:  Dita
P.O. Box:  Dita
City:  Dita
State:  Dita
Country:  Dita
Zip Code:  Dita

Application for Equipment Authorization FCC Form 731 TCB Version


Applicant Information
Applicant's complete, legal business name: Stryker Medical
FCC Registration Number (FRN): 0017033432
Alphanumeric FCC ID: Z7AB7000
Unique Application Identifier: H8NSXcqI9zkKotaNd4CpQg==
Line one: 3800 East Centre Ave
City: Portage
State: Michigan
Country: United States
Zip Code: 49002

TCB Information
TCB Application Email Address: tcb_admin@intertek.com
TCB Scope: A4: UNII devices & low power transmitters using spread spectrum techniques

FCC ID
Grantee Code: Z7A
Product Code: B7000

Person at the applicant's address to receive grant or for contact
Name: Divya Murali
Title: Director, Global Regulatory Affairs
Telephone Number: 2695678254 Extension:
Fax Number: 2693851062
Email: divya.murali@stryker.com

Technical Contact
Firm Name:
Stryker Medical
First Name: Lionel
Last Name: Gabrillo
Line 1:
3030 Orchard Pkwy
City: San Jose
State: California
Country:
United States
Zip Code: 95134
Telephone Number:
408-833-6543

Extension:
E-Mail:

Non Technical Contact
Firm Name: Stryker Medical
First Name: Roc
Last Name: Jiang
Line 1: 3030 Orchard Pkwy
City: San Jose
State: California
Country: United States
Zip Code: 95134
Telephone Number: 510-240-0517 Extension:
E-Mail: Roc.jiang@stryker.com

Long-Term Confidentiality
Does this application include a request for confidentiality for any portion(s) of the data contained in this application pursuant to 47 CFR § 0.459 of the Commission Rules?:   Yes

Short-Term Confidentiality
Does short-term confidentiality apply to this application?:   No
If so, specify the short-term confidentiality release date (MM/DD/YYYY format):  
Note: If no date is supplied, the release date will be set to 45 calendar days past the date of grant.

Software Defined/Cognitive Radio
Is this application for software defined/cognitive radio authorization?   Yes

Equipment Class
Equipment Class:   DTS - Digital Transmission System
Description of product as it is marketed: (NOTE: This text will appear below the equipment class on the grant): Communication Module

Related OET KnowledgeDataBase Inquiry
Is there a KDB inquiry associated with this application?  Yes

Modular Equipment
Modular Type:  Single Modular Approval

Application Purpose
Application is for:   Change in identification of presently authorized equipment. Original FCC ID: VPYLBEE5XV2EA Grant Date: 08/19/2023

Composite/Related Equipment
Is the equipment in this application a composite device subject to an additional equipment authorization?   Yes
Is the equipment in this application part of a system that operates with, or is marketed with, another device that requires an equipment authorization?   No


Test Firm Information
Name of test firm and contact person on file with the FCC:
Firm Name:   SGS Taiwan Ltd. Central RF Lab
First Name:   Ryan
Last Name:   WANG
Telephone Number: 886222993279 Extension: 1473
E-mail:  ryan-ec.wang@sgs.com

Grant Comments
Enter any text that you would like to appear at the bottom of the Grant of Equipment Authorization:
Limited Module Approval Software Defined Radio. Output Power listed is the maximum conducted output power. This device must be installed and operated so as to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi-transmitter product procedures, or as evaluated in this filing. This device supports 20 and 40 MHz.
Set the grant of this application to be deferred to a specified date:
No

Equipment Authorization Waiver
Is there an equipment authorization waiver associated with this application?  No
If there is an equipment authorization waiver associated with this application, has the associated waiver been approved and all information uploaded?:  No

WILLFUL FALSE STATEMENTS MADE ON THIS FORM ARE PUNISHABLE BY FINE AND IMPRISONMENT (U.S. CODE, TITLE 18, SECTION 1001), AND/OR REVOCATION OF ANY STATION LICENSE OR CONSTRUCTION PERMIT (U.S. CODE, TITLE 47, SECTION 312(a)(1)), AND/OR FORFEITURE (U.S. CODE, TITLE 47, SECTION 503).

SECTION 5301 (ANTI-DRUG ABUSE) CERTIFICATION:
The applicant must certify that neither the applicant nor any party to the application is subject to a denial of Federal benefits, that include FCC benefits, pursuant to Section 5301 of the Anti-Drug Abuse Act of 1988, 21 U.S.C. § 862 because of a conviction for possession or distribution of a controlled substance. See 47 CFR 1.2002(b) for the definition of a "party" for these purposes.

Does the applicant or authorized agent so certify?  Yes

Applicant/Agent Certification:

I certify that I am authorized to sign this application. All of the statements herein and the exhibits attached hereto, are true and correct to the best of my knowledge and belief. In accepting a Grant of Equipment Authorization as a result of the representations made in this application, the applicant is responsible for (1) labeling the equipment with the exact FCC ID specified in this application, (2) compliance statement labeling pursuant to the applicable rules, and (3) compliance of the equipment with the applicable technical rules. If the applicant is not the actual manufacturer of the equipment, appropriate arrangements have been made with the manufacturer to ensure that production units of this equipment will continue to comply with the FCC's technical requirements.

Authorizing an agent to sign this application, is done solely at the applicant's discretion; however, the applicant remains responsible for all statements in this application.

If an agent has signed this application on behalf of the applicant, a written letter of authorization which includes information to enable the agent to respond to the above section 5301 (Anti-Drug Abuse) Certification statement has been provided by the applicant. It is understood that the letter of authorization must be submitted to the FCC upon request, and that the FCC reserves the right to contact the applicant directly at any time.

Signature of Authorized Person Filing:  Dita Pual
Title of authorized signature:  Director RAQA Digital Health

Complete items below if agent signs the application:

Firm Name:  Stryker Medical
Name:  Dita Dita Dita
Line 1:  Dita
Line 2:  Dita
P.O. Box:  Dita
City:  Dita
State:  Dita
Country:  Dita
Zip Code:  Dita

Application for Equipment Authorization FCC Form 731 TCB Version


Applicant Information
Applicant's complete, legal business name: Stryker Medical
FCC Registration Number (FRN): 0017033432
Alphanumeric FCC ID: Z7AB7000
Unique Application Identifier: /zCPb5YhdwL/fS3R3wzJ2g==
Line one: 3800 East Centre Ave
City: Portage
State: Michigan
Country: United States
Zip Code: 49002

TCB Information
TCB Application Email Address: tcb_admin@intertek.com
TCB Scope: A4: UNII devices & low power transmitters using spread spectrum techniques

FCC ID
Grantee Code: Z7A
Product Code: B7000

Person at the applicant's address to receive grant or for contact
Name: Divya Murali
Title: Director, Global Regulatory Affairs
Telephone Number: 2695678254 Extension:
Fax Number: 2693851062
Email: divya.murali@stryker.com

Technical Contact
Firm Name:
Stryker Medical
First Name: Lionel
Last Name: Gabrillo
Line 1:
3030 Orchard Pkwy
City: San Jose
State: California
Country:
United States
Zip Code: 95134
Telephone Number:
408-833-6543

Extension:
E-Mail:

Non Technical Contact
Firm Name: Stryker Medical
First Name: Roc
Last Name: Jiang
Line 1: 3030 Orchard Pkwy
City: San Jose
State: California
Country: United States
Zip Code: 95134
Telephone Number: 510-240-0517 Extension:
E-Mail: Roc.jiang@stryker.com

Long-Term Confidentiality
Does this application include a request for confidentiality for any portion(s) of the data contained in this application pursuant to 47 CFR § 0.459 of the Commission Rules?:   No

Short-Term Confidentiality
Does short-term confidentiality apply to this application?:   No
If so, specify the short-term confidentiality release date (MM/DD/YYYY format):  
Note: If no date is supplied, the release date will be set to 45 calendar days past the date of grant.

Software Defined/Cognitive Radio
Is this application for software defined/cognitive radio authorization?   Yes

Equipment Class
Equipment Class:   6ID - 15E 6 GHz Low Power Indoor Access Point
Description of product as it is marketed: (NOTE: This text will appear below the equipment class on the grant): Communication Module

Related OET KnowledgeDataBase Inquiry
Is there a KDB inquiry associated with this application?  Yes

Modular Equipment
Modular Type:  Single Modular Approval

Application Purpose
Application is for:   Change in identification of presently authorized equipment. Original FCC ID: VPYLBEE5XV2EA Grant Date: 08/19/2023

Composite/Related Equipment
Is the equipment in this application a composite device subject to an additional equipment authorization?   Yes
Is the equipment in this application part of a system that operates with, or is marketed with, another device that requires an equipment authorization?   No


Test Firm Information
Name of test firm and contact person on file with the FCC:
Firm Name:   SGS Taiwan Ltd. Central RF Lab
First Name:   Ryan
Last Name:   WANG
Telephone Number: 886222993279 Extension: 1473
E-mail:  ryan-ec.wang@sgs.com

Grant Comments
Enter any text that you would like to appear at the bottom of the Grant of Equipment Authorization:
Limited Module Approval Software Defined Radio. Output Power listed is the maximum conducted output power. This device must be installed and operated so as to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi-transmitter product procedures, or as evaluated in this filing. This device supports 20, 40 , 80 and 160 MHz modes. Restricted to indoor use only in 6GHz band
Set the grant of this application to be deferred to a specified date:
No

Equipment Authorization Waiver
Is there an equipment authorization waiver associated with this application?  No
If there is an equipment authorization waiver associated with this application, has the associated waiver been approved and all information uploaded?:  No

WILLFUL FALSE STATEMENTS MADE ON THIS FORM ARE PUNISHABLE BY FINE AND IMPRISONMENT (U.S. CODE, TITLE 18, SECTION 1001), AND/OR REVOCATION OF ANY STATION LICENSE OR CONSTRUCTION PERMIT (U.S. CODE, TITLE 47, SECTION 312(a)(1)), AND/OR FORFEITURE (U.S. CODE, TITLE 47, SECTION 503).

SECTION 5301 (ANTI-DRUG ABUSE) CERTIFICATION:
The applicant must certify that neither the applicant nor any party to the application is subject to a denial of Federal benefits, that include FCC benefits, pursuant to Section 5301 of the Anti-Drug Abuse Act of 1988, 21 U.S.C. § 862 because of a conviction for possession or distribution of a controlled substance. See 47 CFR 1.2002(b) for the definition of a "party" for these purposes.

Does the applicant or authorized agent so certify?  Yes

Applicant/Agent Certification:

I certify that I am authorized to sign this application. All of the statements herein and the exhibits attached hereto, are true and correct to the best of my knowledge and belief. In accepting a Grant of Equipment Authorization as a result of the representations made in this application, the applicant is responsible for (1) labeling the equipment with the exact FCC ID specified in this application, (2) compliance statement labeling pursuant to the applicable rules, and (3) compliance of the equipment with the applicable technical rules. If the applicant is not the actual manufacturer of the equipment, appropriate arrangements have been made with the manufacturer to ensure that production units of this equipment will continue to comply with the FCC's technical requirements.

Authorizing an agent to sign this application, is done solely at the applicant's discretion; however, the applicant remains responsible for all statements in this application.

If an agent has signed this application on behalf of the applicant, a written letter of authorization which includes information to enable the agent to respond to the above section 5301 (Anti-Drug Abuse) Certification statement has been provided by the applicant. It is understood that the letter of authorization must be submitted to the FCC upon request, and that the FCC reserves the right to contact the applicant directly at any time.

Signature of Authorized Person Filing:  Dita Paul
Title of authorized signature:  Director RAQA Digital Health

Complete items below if agent signs the application:

Firm Name:  Stryker Medical
Name:  Dita Dita Dita
Line 1:  Dita
Line 2:  Dita
P.O. Box:  Dita
City:  Dita
State:  Dita
Country:  Dita
Zip Code:  Dita

Applications are submitted for FCC ID and Grant requests. Click an above application to view details

Grants

TCB GRANT OF EQUIPMENT
AUTHORIZATION
TCB
Certification
Issued Under the Authority of the
Federal Communications Commission
By:

  Intertek Testing Services NA, Inc.
70 Codman Hill Road
Boxborough, MA 01719
Date of Grant: 03/14/2025

Application Dated: 02/27/2025
Stryker Medical
3800 East Centre Ave
Portage, MI 49002
 
Attention: Divya Murali , Director, Global Regulatory Affairs

NOT TRANSFERABLE
EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below.
 
FCC IDENTIFIER:  Z7AB7000
Name of Grantee:  Stryker Medical
Equipment Class: 15E 6 GHz Low Power Indoor Access Point
Notes: Communication Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC MO 15E 5955.0  -  7095.0 0.095  

Limited Module Approval Software Defined Radio. Output Power listed is the maximum conducted output power. This device must be installed and operated so as to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi-transmitter product procedures, or as evaluated in this filing. This device supports 20, 40 , 80 and 160 MHz modes. Restricted to indoor use only in 6GHz band

CC: This device is certified pursuant to two different Part 15 rules sections.
MO: This Multiple Input Multiple Output (MIMO) device was evaluated for multiple transmitted signals as indicated in the filing.
COPY FEDERAL COMMUNICATIONS
COMMISSION
WASHINGTON, D.C. 20554

GRANT OF EQUIPMENT
AUTHORIZATION
COPY
Certification

Stryker Medical
3800 East Centre Ave
Portage, MI 49002
United States
  Date of Grant: 03/14/2025

Application Dated: 02/27/2025
 
Attention: Divya Murali , Director, Global Regulatory Affairs

NOT TRANSFERABLE
EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below.
 
FCC IDENTIFIER:  Z7AB7000
Name of Grantee:  Stryker Medical
Equipment Class: 15E 6 GHz Low Power Indoor Access Point
Notes: Communication Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC MO 15E 5955.0  -  7095.0 0.095  

Limited Module Approval Software Defined Radio. Output Power listed is the maximum conducted output power. This device must be installed and operated so as to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi-transmitter product procedures, or as evaluated in this filing. This device supports 20, 40 , 80 and 160 MHz modes. Restricted to indoor use only in 6GHz band


CC: This device is certified pursuant to two different Part 15 rules sections.
MO: This Multiple Input Multiple Output (MIMO) device was evaluated for multiple transmitted signals as indicated in the filing.

Mail To:


EA973652
TCB GRANT OF EQUIPMENT
AUTHORIZATION
TCB
Certification
Issued Under the Authority of the
Federal Communications Commission
By:

  Intertek Testing Services NA, Inc.
70 Codman Hill Road
Boxborough, MA 01719
Date of Grant: 03/14/2025

Application Dated: 02/27/2025
Stryker Medical
3800 East Centre Ave
Portage, MI 49002
 
Attention: Divya Murali , Director, Global Regulatory Affairs

NOT TRANSFERABLE
EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below.
 
FCC IDENTIFIER:  Z7AB7000
Name of Grantee:  Stryker Medical
Equipment Class: Digital Transmission System
Notes: Communication Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC MO 15C 2402.0  -  2480.0 0.012  
CC MO 15C 2412.0  -  2462.0 0.497  

Limited Module Approval Software Defined Radio. Output Power listed is the maximum conducted output power. This device must be installed and operated so as to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi-transmitter product procedures, or as evaluated in this filing. This device supports 20 and 40 MHz.

CC: This device is certified pursuant to two different Part 15 rules sections.
MO: This Multiple Input Multiple Output (MIMO) device was evaluated for multiple transmitted signals as indicated in the filing.
COPY FEDERAL COMMUNICATIONS
COMMISSION
WASHINGTON, D.C. 20554

GRANT OF EQUIPMENT
AUTHORIZATION
COPY
Certification

Stryker Medical
3800 East Centre Ave
Portage, MI 49002
United States
  Date of Grant: 03/14/2025

Application Dated: 02/27/2025
 
Attention: Divya Murali , Director, Global Regulatory Affairs

NOT TRANSFERABLE
EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below.
 
FCC IDENTIFIER:  Z7AB7000
Name of Grantee:  Stryker Medical
Equipment Class: Digital Transmission System
Notes: Communication Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC MO 15C 2402.0  -  2480.0 0.012  
CC MO 15C 2412.0  -  2462.0 0.497  

Limited Module Approval Software Defined Radio. Output Power listed is the maximum conducted output power. This device must be installed and operated so as to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi-transmitter product procedures, or as evaluated in this filing. This device supports 20 and 40 MHz.


CC: This device is certified pursuant to two different Part 15 rules sections.
MO: This Multiple Input Multiple Output (MIMO) device was evaluated for multiple transmitted signals as indicated in the filing.

Mail To:


EA937969
TCB GRANT OF EQUIPMENT
AUTHORIZATION
TCB
Certification
Issued Under the Authority of the
Federal Communications Commission
By:

  Intertek Testing Services NA, Inc.
70 Codman Hill Road
Boxborough, MA 01719
Date of Grant: 03/14/2025

Application Dated: 02/27/2025
Stryker Medical
3800 East Centre Ave
Portage, MI 49002
 
Attention: Divya Murali , Director, Global Regulatory Affairs

NOT TRANSFERABLE
EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below.
 
FCC IDENTIFIER:  Z7AB7000
Name of Grantee:  Stryker Medical
Equipment Class: Unlicensed National Information Infrastructure TX
Notes: Communication Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC MO 15E 5180.0  -  5240.0 0.063  
CC MO 15E 5260.0  -  5320.0 0.062  
CC MO 15E 5500.0  -  5720.0 0.061  
CC MO 15E 5745.0  -  5825.0 0.063  

Limited Module Approval Software Defined Radio. Output Power listed is the maximum conducted output power. This device must be installed and operated so as to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi-transmitter product procedures, or as evaluated in this filing. This device supports 20, 40 , and 80 MHz modes. Restricted to indoor use only in 6GHz band. Operation in the 5250-5350 MHz and 5470 - 5725MHz limited to Client only operation.

CC: This device is certified pursuant to two different Part 15 rules sections.
MO: This Multiple Input Multiple Output (MIMO) device was evaluated for multiple transmitted signals as indicated in the filing.
COPY FEDERAL COMMUNICATIONS
COMMISSION
WASHINGTON, D.C. 20554

GRANT OF EQUIPMENT
AUTHORIZATION
COPY
Certification

Stryker Medical
3800 East Centre Ave
Portage, MI 49002
United States
  Date of Grant: 03/14/2025

Application Dated: 02/27/2025
 
Attention: Divya Murali , Director, Global Regulatory Affairs

NOT TRANSFERABLE
EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below.
 
FCC IDENTIFIER:  Z7AB7000
Name of Grantee:  Stryker Medical
Equipment Class: Unlicensed National Information Infrastructure TX
Notes: Communication Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC MO 15E 5180.0  -  5240.0 0.063  
CC MO 15E 5260.0  -  5320.0 0.062  
CC MO 15E 5500.0  -  5720.0 0.061  
CC MO 15E 5745.0  -  5825.0 0.063  

Limited Module Approval Software Defined Radio. Output Power listed is the maximum conducted output power. This device must be installed and operated so as to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi-transmitter product procedures, or as evaluated in this filing. This device supports 20, 40 , and 80 MHz modes. Restricted to indoor use only in 6GHz band. Operation in the 5250-5350 MHz and 5470 - 5725MHz limited to Client only operation.


CC: This device is certified pursuant to two different Part 15 rules sections.
MO: This Multiple Input Multiple Output (MIMO) device was evaluated for multiple transmitted signals as indicated in the filing.

Mail To:


EA557912
TCB GRANT OF EQUIPMENT
AUTHORIZATION
TCB
Certification
Issued Under the Authority of the
Federal Communications Commission
By:

  Intertek Testing Services NA, Inc.
70 Codman Hill Road
Boxborough, MA 01719
Date of Grant: 03/14/2025

Application Dated: 02/27/2025
Stryker Medical
3800 East Centre Ave
Portage, MI 49002
 
Attention: Divya Murali , Director, Global Regulatory Affairs

NOT TRANSFERABLE
EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below.
 
FCC IDENTIFIER:  Z7AB7000
Name of Grantee:  Stryker Medical
Equipment Class: Part 15 Spread Spectrum Transmitter
Notes: Communication Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC MO 15C 2402.0  -  2480.0 0.011  

Limited Module Approval Software Defined Radio. Output Power listed is the maximum conducted output power. This device must be installed and operated so as to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi-transmitter product procedures, or as evaluated in this filing.

CC: This device is certified pursuant to two different Part 15 rules sections.
MO: This Multiple Input Multiple Output (MIMO) device was evaluated for multiple transmitted signals as indicated in the filing.
COPY FEDERAL COMMUNICATIONS
COMMISSION
WASHINGTON, D.C. 20554

GRANT OF EQUIPMENT
AUTHORIZATION
COPY
Certification

Stryker Medical
3800 East Centre Ave
Portage, MI 49002
United States
  Date of Grant: 03/14/2025

Application Dated: 02/27/2025
 
Attention: Divya Murali , Director, Global Regulatory Affairs

NOT TRANSFERABLE
EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below.
 
FCC IDENTIFIER:  Z7AB7000
Name of Grantee:  Stryker Medical
Equipment Class: Part 15 Spread Spectrum Transmitter
Notes: Communication Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC MO 15C 2402.0  -  2480.0 0.011  

Limited Module Approval Software Defined Radio. Output Power listed is the maximum conducted output power. This device must be installed and operated so as to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi-transmitter product procedures, or as evaluated in this filing.


CC: This device is certified pursuant to two different Part 15 rules sections.
MO: This Multiple Input Multiple Output (MIMO) device was evaluated for multiple transmitted signals as indicated in the filing.

Mail To:


EA936621
TCB GRANT OF EQUIPMENT
AUTHORIZATION
TCB
Certification
Issued Under the Authority of the
Federal Communications Commission
By:

  Intertek Testing Services NA, Inc.
70 Codman Hill Road
Boxborough, MA 01719
Date of Grant: 03/14/2025

Application Dated: 02/27/2025
Stryker Medical
3800 East Centre Ave
Portage, MI 49002
 
Attention: Divya Murali , Director, Global Regulatory Affairs

NOT TRANSFERABLE
EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below.
 
FCC IDENTIFIER:  Z7AB7000
Name of Grantee:  Stryker Medical
Equipment Class: 15E 6 GHz Low Power Indoor Client
Notes: Communication Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC MO 15E 5955.0  -  7095.0 0.024  

Limited Module Approval Software Defined Radio. Output Power listed is the maximum conducted output power. This device must be installed and operated so as to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi-transmitter product procedures, or as evaluated in this filing. This device supports 20, 40 , 80 and 160 MHz modes. Restricted to indoor use only in 6GHz band

CC: This device is certified pursuant to two different Part 15 rules sections.
MO: This Multiple Input Multiple Output (MIMO) device was evaluated for multiple transmitted signals as indicated in the filing.
COPY FEDERAL COMMUNICATIONS
COMMISSION
WASHINGTON, D.C. 20554

GRANT OF EQUIPMENT
AUTHORIZATION
COPY
Certification

Stryker Medical
3800 East Centre Ave
Portage, MI 49002
United States
  Date of Grant: 03/14/2025

Application Dated: 02/27/2025
 
Attention: Divya Murali , Director, Global Regulatory Affairs

NOT TRANSFERABLE
EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below.
 
FCC IDENTIFIER:  Z7AB7000
Name of Grantee:  Stryker Medical
Equipment Class: 15E 6 GHz Low Power Indoor Client
Notes: Communication Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC MO 15E 5955.0  -  7095.0 0.024  

Limited Module Approval Software Defined Radio. Output Power listed is the maximum conducted output power. This device must be installed and operated so as to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi-transmitter product procedures, or as evaluated in this filing. This device supports 20, 40 , 80 and 160 MHz modes. Restricted to indoor use only in 6GHz band


CC: This device is certified pursuant to two different Part 15 rules sections.
MO: This Multiple Input Multiple Output (MIMO) device was evaluated for multiple transmitted signals as indicated in the filing.

Mail To:


EA678497

Grants authorize equipment for operation at approved frequencies and sale within the USA. Click an above grant to view details