FCC ID Z7A-SDMAN

SDIO Wireless Module

by Stryker Medical

Grantee Code: Z7A   Product Code: SDMAN
Latest application date: 2016-04-12

Device Images

FCC ID Device Details

FCC IDZ7A-SDMAN
Mirrorsfcc.id | gov | fccid.ai
Grantee CodeZ7A
Product CodeSDMAN
Applicant BusinessStryker Medical 🇺🇸
Related Domains stryker.com
Equipment ClassSDIO Wireless Module
Test FirmBureau Veritas Consumer Products Services, Inc.

Operating Frequencies

Frequency RangeApplication PurposeFinal Action Date
5180-5240 MHzClass II permissive change or modification of presently authorized equipment2016-04-12
2412-2462 MHzClass II permissive change or modification of presently authorized equipment2016-04-12
2402-2480 MHzChange in identification of presently authorized equipment. Original FCC ID: N6C-SDMAN Grant Date: 09/14/20152016-03-24
5180-5320 MHzChange in identification of presently authorized equipment. Original FCC ID: N6C-SDMAN Grant Date: 09/14/20152016-03-24

Exhibits

DocumentTypeAvailableFile
Users ManualUsers Manual2016-03-24PDF 158 KB
Users manualUsers Manual2016-03-24PDF 158 KB
Internal PhotosInternal Photos2016-04-12PDF 212.5 KB
Host External PhotosExternal Photos2016-04-12PDF 170 KB
External PhotosExternal Photos2016-03-24PDF 125.1 KB
LabelID Label/Location Info2016-03-24PDF 299.6 KB
Test Setup PhotosTest Setup Photos2016-04-12PDF 132.3 KB
SAR Test ReportRF Exposure Info2016-04-12PDF 3.6 MB
Test ReportTest Report2016-04-12PDF 3.6 MB
Permissive Change LetterCover Letter(s)2016-04-12PDF 305.5 KB
Product Certification Rep Auth LetterCover Letter(s)2016-04-12PDF 349.1 KB
Change of ID Request Letter from Orig. ApplicantCover Letter(s)2016-03-24PDF 155.7 KB
Change of ID request LetterCover Letter(s)2016-03-24PDF 340.7 KB

Application Information

Application IDaz1Cd7bfzrmcgEY4AKakew==
Final Action Date2016-04-12
Application PurposeClass II permissive change or modification of presently authorized equipment
Applicant FRN0021243142
ModelSDMAN
Frequency Range5180-5240 MHz
Equipment ClassNII - Unlicensed National Information Infrastructure TX
Device DescriptionSDIO Wireless Module
Responsible PartyMichael Hayes, Sr Principle EE, mike.hayes@stryker.com , 2693896754
Test FirmSarb Shelopal, Bureau Veritas Consumer Products Services, Inc., Sarbjit.Shelopal@bureauveritas.com , +1 925 963 4420
TCB Emailtcb@siemic.com
TCB ScopeA4: UNII devices & low power transmitters using spread spectrum techniques
Short-Term ConfidentialityNo
Long-Term ConfidentialityNo
Grant DeferralNo
Modular EquipmentSingle Modular Approval
Composite DeviceYes
Composite PartNo
Cognitive RadioNo
Authorization WaiverNo
Authorization Waiver ApprovedNo
Section 5301 CertificationYes
Related OET Knowledge DataBase InquiryNo
Grant CommentsCIIPC to add RF category Portable SAR results when module is used in portable host Stryker Bed System. The highest reported SAR values found during evaluation is: Body: Body: 1.337 W/kg. BT function is disabled. Single Modular Approval. Output power listed is Conducted. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrator and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrator are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter except the conditions shown in this filing and/or in accordance with FCC multi-transmitter product guidelines. OEM integrator must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter. This device complies with the Dynamic Frequency Selection (DFS) requirements of Report and KDB 905462 D03 as a Client only without Radar Detection.

Applications

Application IDDatePurpose
az1Cd7bfzrmcgEY4AKakew==2016-04-12Class II permissive change or modification of presently authorized equipment
RHA5GJlaZ/+c7QvbyF/L7w==2016-04-12Class II permissive change or modification of presently authorized equipment
xzjpy2aMLsPMfXjoU7gT5g==2016-03-24Change in identification of presently authorized equipment. Original FCC ID: N6C-SDMAN Grant Date: 09/14/2015
EAq5YdMSkk4h/sRuRhEfAQ==2016-03-24Change in identification of presently authorized equipment. Original FCC ID: N6C-SDMAN Grant Date: 09/14/2015

Equipment Authorization

FrequencyOutputRulesGrant Notes
2402-2480 MHz0.008615CCC
2412-2462 MHz0.173000015CCC
2412-2462 MHz0.17315CCC
5180-5240 MHz0.024715E38, CC
5180-5320 MHz0.024715E38, CC, ND
5260-5320 MHz0.024715E38, CC, ND
5500-5580 MHz0.01815E38, CC, ND
5660-5700 MHz0.0215E38, CC, ND
5745-5825 MHz0.024215E38, CC

Grants

TCB Grant - Application xzjpy2aMLsPMfXjoU7gT5g==

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

  Siemic Inc.
775 Montague Expressway
Milpitas, CA 95035
Date of Grant: 03/24/2016

Application Dated: 03/23/2016
Stryker Medical
3800 East Centre Ave
Portage, MI 49002
 
Attention: Michael Hayes , Sr Principle EE

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:  Z7A-SDMAN
Name of Grantee:  Stryker Medical
Equipment Class: Digital Transmission System
Notes: SDIO Wireless Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC 15C 2412.0  -  2462.0 0.173  
CC 15C 2402.0  -  2480.0 0.0086  

Single Modular Approval. Output power listed is Conducted. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter. OEM integrators must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter.

CC: This device is certified pursuant to two different Part 15 rules sections.

EAS Grant - Application xzjpy2aMLsPMfXjoU7gT5g==

COPY FEDERAL COMMUNICATIONS
COMMISSION
WASHINGTON, D.C. 20554

GRANT OF EQUIPMENT
AUTHORIZATION
COPY
Certification

Stryker Medical
3800 East Centre Ave P.O. Box ,
Portage, MI 49002
United States
  Date of Grant: 03/24/2016

Application Dated: 03/23/2016
 
Attention: Michael Hayes , Sr Principle EE

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:  Z7A-SDMAN
Name of Grantee:  Stryker Medical
Equipment Class: Digital Transmission System
Notes: SDIO Wireless Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC 15C 2412.0  -  2462.0 0.173  
CC 15C 2402.0  -  2480.0 0.0086  

Single Modular Approval. Output power listed is Conducted. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter. OEM integrators must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter.


CC: This device is certified pursuant to two different Part 15 rules sections.

TCB Grant - Application RHA5GJlaZ/+c7QvbyF/L7w==

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

  Bureau Veritas Consumer Products Services, Inc.
775 Montague Expressway
Milpitas, CA 95035
Date of Grant: 04/12/2016

Application Dated: 04/12/2016
Stryker Medical
3800 East Centre Ave
Portage, MI 49002
 
Attention: Michael Hayes , Sr Principle EE

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:  Z7A-SDMAN
Name of Grantee:  Stryker Medical
Equipment Class: Digital Transmission System
Notes: SDIO Wireless Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC 15C 2412.0  -  2462.0 0.173  

CIIPC to add RF category Portable SAR results when module is used in portable host Stryker Bed System. The highest reported SAR values found during evaluation is: Body: 0.962 W/kg. BT function is disabled.

Single Modular Approval. Output power listed is Conducted. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrator and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrator are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter. OEM integrator must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter.


CC: This device is certified pursuant to two different Part 15 rules sections.

EAS Grant - Application RHA5GJlaZ/+c7QvbyF/L7w==

COPY FEDERAL COMMUNICATIONS
COMMISSION
WASHINGTON, D.C. 20554

GRANT OF EQUIPMENT
AUTHORIZATION
COPY
Certification

Stryker Medical
3800 East Centre Ave P.O. Box ,
Portage, MI 49002
United States
  Date of Grant: 04/12/2016

Application Dated: 04/12/2016
 
Attention: Michael Hayes , Sr Principle EE

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:  Z7A-SDMAN
Name of Grantee:  Stryker Medical
Equipment Class: Digital Transmission System
Notes: SDIO Wireless Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC 15C 2412.0  -  2462.0 0.173  

CIIPC to add RF category Portable SAR results when module is used in portable host Stryker Bed System. The highest reported SAR values found during evaluation is: Body: 0.962 W/kg. BT function is disabled.

Single Modular Approval. Output power listed is Conducted. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrator and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrator are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter. OEM integrator must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter.


CC: This device is certified pursuant to two different Part 15 rules sections.

TCB Grant - Application EAq5YdMSkk4h/sRuRhEfAQ==

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

  Siemic Inc.
775 Montague Expressway
Milpitas, CA 95035
Date of Grant: 03/24/2016

Application Dated: 03/23/2016
Stryker Medical
3800 East Centre Ave
Portage, MI 49002
 
Attention: Michael Hayes , Sr Principle EE

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:  Z7A-SDMAN
Name of Grantee:  Stryker Medical
Equipment Class: Unlicensed National Information Infrastructure TX
Notes: SDIO Wireless Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
38 CC ND 15E 5180.0  -  5320.0 0.0247  
38 CC ND 15E 5500.0  -  5580.0 0.018  
38 CC ND 15E 5660.0  -  5700.0 0.02  
38 CC 15E 5745.0  -  5825.0 0.0242  

Single Modular Approval. Output power listed is Conducted. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter except the conditions shown in this filing and/or in accordance with FCC multi-transmitter product guidelines. OEM integrators must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter. This device complies with the Dynamic Frequency Selection (DFS) requirements of Report and KDB 905462 D03 as a Client only without Radar Detection

38: This device has shown compliance, in all grant-listed U-NII sub-bands, with the new rules for U-NII devices adopted under Docket No. 13-49 and may be marketed, manufactured, installed or imported after the June 1, 2016 transition deadline.
CC: This device is certified pursuant to two different Part 15 rules sections.
ND: This UNII device complies with the Transmit Power Control (TPC) and Dynamic Frequency Selection (DFS) requirements in Section 15.407(h).

EAS Grant - Application EAq5YdMSkk4h/sRuRhEfAQ==

COPY FEDERAL COMMUNICATIONS
COMMISSION
WASHINGTON, D.C. 20554

GRANT OF EQUIPMENT
AUTHORIZATION
COPY
Certification

Stryker Medical
3800 East Centre Ave P.O. Box ,
Portage, MI 49002
United States
  Date of Grant: 03/24/2016

Application Dated: 03/23/2016
 
Attention: Michael Hayes , Sr Principle EE

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:  Z7A-SDMAN
Name of Grantee:  Stryker Medical
Equipment Class: Unlicensed National Information Infrastructure TX
Notes: SDIO Wireless Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
38 CC ND 15E 5180.0  -  5320.0 0.0247  
38 CC ND 15E 5500.0  -  5580.0 0.018  
38 CC ND 15E 5660.0  -  5700.0 0.02  
38 CC 15E 5745.0  -  5825.0 0.0242  

Single Modular Approval. Output power listed is Conducted. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter except the conditions shown in this filing and/or in accordance with FCC multi-transmitter product guidelines. OEM integrators must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter. This device complies with the Dynamic Frequency Selection (DFS) requirements of Report and KDB 905462 D03 as a Client only without Radar Detection


38: This device has shown compliance, in all grant-listed U-NII sub-bands, with the new rules for U-NII devices adopted under Docket No. 13-49 and may be marketed, manufactured, installed or imported after the June 1, 2016 transition deadline.
CC: This device is certified pursuant to two different Part 15 rules sections.
ND: This UNII device complies with the Transmit Power Control (TPC) and Dynamic Frequency Selection (DFS) requirements in Section 15.407(h).

TCB Grant - Application az1Cd7bfzrmcgEY4AKakew==

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

  Bureau Veritas Consumer Products Services, Inc.
775 Montague Expressway
Milpitas, CA 95035
Date of Grant: 04/12/2016

Application Dated: 04/12/2016
Stryker Medical
3800 East Centre Ave
Portage, MI 49002
 
Attention: Michael Hayes , Sr Principle EE

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:  Z7A-SDMAN
Name of Grantee:  Stryker Medical
Equipment Class: Unlicensed National Information Infrastructure TX
Notes: SDIO Wireless Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
38 CC 15E 5180.0  -  5240.0 0.0247  
38 CC ND 15E 5260.0  -  5320.0 0.0247  
38 CC ND 15E 5500.0  -  5580.0 0.018  
38 CC ND 15E 5660.0  -  5700.0 0.02  
38 CC 15E 5745.0  -  5825.0 0.0242  

CIIPC to add RF category Portable SAR results when module is used in portable host Stryker Bed System. The highest reported SAR values found during evaluation is: Body: Body: 1.337 W/kg. BT function is disabled.

Single Modular Approval. Output power listed is Conducted. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrator and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrator are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter except the conditions shown in this filing and/or in accordance with FCC multi-transmitter product guidelines. OEM integrator must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter. This device complies with the Dynamic Frequency Selection (DFS) requirements of Report and KDB 905462 D03 as a Client only without Radar Detection.


38: This device has shown compliance, in all grant-listed U-NII sub-bands, with the new rules for U-NII devices adopted under Docket No. 13-49 and may be marketed, manufactured or imported after the June 1, 2016 transition deadline.
CC: This device is certified pursuant to two different Part 15 rules sections.
ND: This UNII device complies with the Transmit Power Control (TPC) and Dynamic Frequency Selection (DFS) requirements in Section 15.407(h).

EAS Grant - Application az1Cd7bfzrmcgEY4AKakew==

COPY FEDERAL COMMUNICATIONS
COMMISSION
WASHINGTON, D.C. 20554

GRANT OF EQUIPMENT
AUTHORIZATION
COPY
Certification

Stryker Medical
3800 East Centre Ave P.O. Box ,
Portage, MI 49002
United States
  Date of Grant: 04/12/2016

Application Dated: 04/12/2016
 
Attention: Michael Hayes , Sr Principle EE

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:  Z7A-SDMAN
Name of Grantee:  Stryker Medical
Equipment Class: Unlicensed National Information Infrastructure TX
Notes: SDIO Wireless Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
38 CC 15E 5180.0  -  5240.0 0.0247  
38 CC ND 15E 5260.0  -  5320.0 0.0247  
38 CC ND 15E 5500.0  -  5580.0 0.018  
38 CC ND 15E 5660.0  -  5700.0 0.02  
38 CC 15E 5745.0  -  5825.0 0.0242  

CIIPC to add RF category Portable SAR results when module is used in portable host Stryker Bed System. The highest reported SAR values found during evaluation is: Body: Body: 1.337 W/kg. BT function is disabled.

Single Modular Approval. Output power listed is Conducted. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrator and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrator are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter except the conditions shown in this filing and/or in accordance with FCC multi-transmitter product guidelines. OEM integrator must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter. This device complies with the Dynamic Frequency Selection (DFS) requirements of Report and KDB 905462 D03 as a Client only without Radar Detection.


38: This device has shown compliance, in all grant-listed U-NII sub-bands, with the new rules for U-NII devices adopted under Docket No. 13-49 and may be marketed, manufactured or imported after the June 1, 2016 transition deadline.
CC: This device is certified pursuant to two different Part 15 rules sections.
ND: This UNII device complies with the Transmit Power Control (TPC) and Dynamic Frequency Selection (DFS) requirements in Section 15.407(h).

Mail To: