FCC ID Z7A-SDMACP
Embedded Wireless module
by Stryker Medical
Grantee Code: Z7A Product Code: SDMACP
Latest application date: 2025-08-27
FCC ID Device Details
Operating Frequencies
| Frequency Range | Application Purpose | Final Action Date |
|---|---|---|
| 5180-5240 MHz | Class II permissive change or modification of presently authorized equipment | 2025-08-27 |
| 2412-2462 MHz | Class II permissive change or modification of presently authorized equipment | 2025-08-27 |
| 2412-2462 MHz | Class II permissive change or modification of presently authorized equipment | 2021-09-15 |
| 5180-5240 MHz | Class II permissive change or modification of presently authorized equipment | 2021-09-15 |
| 5180-5240 MHz | Class II permissive change or modification of presently authorized equipment | 2020-09-03 |
| 2402-2480 MHz | Class II permissive change or modification of presently authorized equipment | 2020-09-03 |
| 5180-5240 MHz | Change in identification of presently authorized equipment. Original FCC ID: N6C-PMACS Grant Date: 08/21/2017 | 2019-10-29 |
| 2402-2480 MHz | Change in identification of presently authorized equipment. Original FCC ID: N6C-PMACS Grant Date: 08/21/2017 | 2019-10-29 |
| 2402-2480 MHz | Change in identification of presently authorized equipment. Original FCC ID: N6C-PMACS Grant Date: 08/21/2017 | 2019-10-29 |
Exhibits
| Document | Type | Available | File |
|---|---|---|---|
| 6507-009-001_revAB.3 | Users Manual | 2025-08-27 | PDF 4 MB |
| 3009-009-001_revA.0 | Users Manual | 2021-03-02 | PDF 3.8 MB |
| Internal Photos | Internal Photos | 2022-03-14 | PDF 178.6 KB |
| Internal Photos_20200511_v1 - Internal photos | Internal Photos | 2021-03-02 | PDF 364.4 KB |
| Module in footboard photos | Internal Photos | 2021-03-02 | PDF 4.6 MB |
| Internal Photos | Internal Photos | 2019-10-29 | PDF 364.4 KB |
| External Photos_20200511_v1 - External photos | External Photos | 2021-03-02 | PDF 274.3 KB |
| Host Photos | External Photos | 2021-03-02 | PDF 3.2 MB |
| External Photos | External Photos | 2019-10-29 | PDF 274.3 KB |
| Label and Label Location | ID Label/Location Info | 2025-08-27 | PDF 278.8 KB |
| Label and Label Location | ID Label/Location Info | 2021-09-15 | PDF 405 KB |
| 300900380012_revAA.0 | ID Label/Location Info | 2020-09-03 | PDF 435.4 KB |
| 300900380013_revAA.0 | ID Label/Location Info | 2020-09-03 | PDF 428.7 KB |
| 3009_bt_label | ID Label/Location Info | 2020-09-03 | PDF 1.5 MB |
| 3009_wifi_label | ID Label/Location Info | 2020-09-03 | PDF 897.3 KB |
| Label Location | ID Label/Location Info | 2019-10-29 | PDF 128.3 KB |
| Product Label | ID Label/Location Info | 2019-10-29 | PDF 28.9 KB |
| R12472704-S1_Appendixes FCC - Part 1a of 2 | Test Setup Photos | 2021-03-02 | PDF 803.2 KB |
| R15147852-E2 v2 FCC BT Spotchecks | Test Report | 2025-08-27 | PDF 929.3 KB |
| R15147852-E5 v2 FCC ISED SIM TX REPORT | Test Report | 2025-08-27 | PDF 1.4 MB |
| Test Report_20210812_v1 - R12464606-S1V1 Hydrogen XT FCC SAR Report | RF Exposure Info | 2021-09-15 | PDF 913.8 KB |
| Test Report_20210812_v1 - R12464606-S1V1_Appendix A | RF Exposure Info | 2021-09-15 | PDF 852.9 KB |
| Test Report_20210812_v1 - R12464606-S1V1_Appendixes B-F | RF Exposure Info | 2021-09-15 | PDF 4.7 MB |
| Test Report_20200511_v1 - R12472704-S1_Appendixes FCC - Part 2 of 2 | RF Exposure Info | 2020-09-03 | PDF 4.3 MB |
| FCC 2.911[d][5] Attestation | Attestation Statements | 2025-08-27 | PDF 139 KB |
| FCC Agent for service Attestation | Attestation Statements | 2025-08-27 | PDF 386.9 KB |
| FCC Agent Auth Letter [UL LLC] | Cover Letter(s) | 2025-08-27 | PDF 947.3 KB |
| FCC Permissive Change Request Letter_Aug 30 2024_signed [002] | Cover Letter(s) | 2025-08-27 | PDF 136.7 KB |
| Cover Letters_20210812_v1 - FCC Agent Authorization Letter | Cover Letter(s) | 2021-09-15 | PDF 150 KB |
| Cover Letters_20210812_v1 - FCC Permissive Change Request Letter Metadata only | Cover Letter(s) | 2021-09-15 | PDF 93.6 KB |
| FCC Authorization Letter Divya Murali | Cover Letter(s) | 2021-09-15 | PDF 16.1 KB |
| FCC Confidentiality edit | Cover Letter(s) | 2021-09-15 | PDF 105.3 KB |
| FCC Permissive Change Request Letter_MTS_dm | Cover Letter(s) | 2021-09-15 | PDF 92.1 KB |
| Cover Letters_20200511_v1 - FCC Agent Authorization Letter [Personalized]_dmsign | Cover Letter(s) | 2020-09-03 | PDF 65.1 KB |
| FCC Confidentiality | Cover Letter(s) | 2020-09-03 | PDF 105.3 KB |
| FCC Permissive Change Request Letter | Cover Letter(s) | 2020-09-03 | PDF 91.7 KB |
| Change of ID Auth Letter | Cover Letter(s) | 2019-10-29 | PDF 683.9 KB |
| Change of ID Request Letter | Cover Letter(s) | 2019-10-29 | PDF 358.6 KB |
| PoA | Cover Letter(s) | 2019-10-29 | PDF 16.1 KB |
| Product Certification Representative Auth Letter | Cover Letter(s) | 2019-10-29 | PDF 296.3 KB |
| R15147852-E3 FCC MPE REPORT | RF Exposure Info | 2025-08-27 | PDF 348.8 KB |
| R12472704-S1 rev2_FCC SAR Report_Stryker 3009 | RF Exposure Info | 2020-09-03 | PDF 853.7 KB |
| R12472704-S1_Appendixes FCC - Part 1b of 2 | RF Exposure Info | 2020-09-03 | PDF 4.7 MB |
| 300900680910_revAB.3 Metadata only | Schematics | PDF 556.2 KB | |
| 521206010900_revAE.0 Metadata only | Schematics | PDF 227 KB | |
| 650700080202_RevAE.0_PCB Metadata only | Schematics | PDF 700.3 KB | |
| Power-PRO 2 Models Metadata only | Operational Description | PDF 35.6 KB |
Application Information
| Application ID | mdeZc5Sj0JzonMDzIoXViA== |
|---|---|
| Final Action Date | 2025-08-27 |
| Application Purpose | Class II permissive change or modification of presently authorized equipment |
| Applicant FRN | 0021243142 |
| Model | SDMACP |
| Frequency Range | 5180-5240 MHz |
| Equipment Class | NII - Unlicensed National Information Infrastructure TX |
| Device Description | Embedded Wireless module |
| Responsible Party | Divya Murali, Director, Global Regulatory Affairs, divya.murali@stryker.com  , 2695678254 |
| Technical Contact | Lariah Sanders, UL LLC, lariah.sanders@ul.com  , 919-549-0945 |
| Test Firm | Steven Thompson, UL LLC, steven.d.thompson@ul.com , 919 549 1430 |
| TCB Email | LST.FRE.CertNotice@ul.com |
| TCB Scope | A4: UNII devices & low power transmitters using spread spectrum techniques |
| Short-Term Confidentiality | No |
| Long-Term Confidentiality | No |
| Grant Deferral | No |
| Modular Equipment | Does not apply |
| Composite Device | Yes |
| Composite Part | No |
| Cognitive Radio | No |
| Authorization Waiver | No |
| Authorization Waiver Approved | No |
| Section 5301 Certification | Yes |
| Related OET Knowledge DataBase Inquiry | No |
| Grant Comments | Class II Permissive Change to allow co-located with Blue Tooth device (FCCID: Z7ALBCA1KU1WA) and disabled Blue Tooth transmitter in FCCID: Z7A-SDMACP. Output power listed is conducted. This grant is valid only when the module is sold to OEM integrators and must be installed by the OEM or OEM integrators. The antennas listed in this application must be installed and not be co-located or operated in conjunction with any other antenna or transmitter. End-users may not be provided with the module installation instructions. OEM integrators and end-users must be provided with transmitter operating conditions for satisfying RF exposure compliance. This device has 20/40/80 MHz bandwidth modes. The 80 MHz mode is limited to channel at 5210MHz, 5290 MHz, 5530 MHz, 5610 MHz, and 5775 MHz. |
Applications
| Application ID | Date | Purpose |
|---|---|---|
| mdeZc5Sj0JzonMDzIoXViA== | 2025-08-27 | Class II permissive change or modification of presently authorized equipment |
| fLjF0YZnRE9wUOUH5xzGWA== | 2025-08-27 | Class II permissive change or modification of presently authorized equipment |
| kHU9dh/Y71qAz0x3IQAAbQ== | 2021-09-15 | Class II permissive change or modification of presently authorized equipment |
| ej2plmNkD9YY5EYichl/zQ== | 2021-09-15 | Class II permissive change or modification of presently authorized equipment |
| X0KspFn6IzM5PFPlzUU2BA== | 2020-09-03 | Class II permissive change or modification of presently authorized equipment |
| 8Hc2mfPGSkINDqO1WeS9Dg== | 2020-09-03 | Class II permissive change or modification of presently authorized equipment |
| uKtYMY/gpdlVc/wpBtRM4Q== | 2019-10-29 | Change in identification of presently authorized equipment. Original FCC ID: N6C-PMACS Grant Date: 08/21/2017 |
| uJUqUwP7JGq4gWUSNGhUlQ== | 2019-10-29 | Change in identification of presently authorized equipment. Original FCC ID: N6C-PMACS Grant Date: 08/21/2017 |
| oTxKQu8e7lwjKKLs4xDq/Q== | 2019-10-29 | Change in identification of presently authorized equipment. Original FCC ID: N6C-PMACS Grant Date: 08/21/2017 |
Equipment Authorization
| Frequency | Output | Rules | Grant Notes |
|---|---|---|---|
| 2402-2480 MHz | 0.2000000 | 15C | CC |
| 2402-2480 MHz | 0.0016 | 15C | CC |
| 2402-2480 MHz | 0.0016000 | 15C | CC |
| 2412-2462 MHz | 0.2000000 | 15C | CC |
| 2412-2462 MHz | 0.2000000 | CC | |
| 2412-2462 MHz | 0.2 | 15C | CC |
| 5180-5240 MHz | 0.013 | 15E | CC |
| 5180-5240 MHz | 0.013 | CC | |
| 5260-5320 MHz | 0.013 | 15E | CC, ND |
| 5260-5320 MHz | 0.013 | CC, ND | |
| 5500-5700 MHz | 0.013 | 15E | CC, ND |
| 5500-5720 MHz | 0.013 | 15E | CC, ND |
| 5500-5700 MHz | 0.013 | CC, ND | |
| 5745-5825 MHz | 0.013 | 15E | CC |
| 5745-5825 MHz | 0.013 | CC |
Grants
TCB Grant - Application X0KspFn6IzM5PFPlzUU2BA==
| TCB | GRANT OF EQUIPMENT AUTHORIZATION |
TCB |
| Certification | ||
| Issued Under the Authority of the | ||
| Federal Communications Commission | ||
| By: |
|
UL Verification Services Inc. (formerly UL CCS) 47173 Benicia Street Fremont, CA 94538 |
Date of Grant: 09/03/2020 Application Dated: 08/26/2020 |
| 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-SDMACP |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Unlicensed National Information Infrastructure TX |
| Notes: | Embedded Wireless module |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15E | 5180.0 - 5240.0 | 0.013 | ||
| CC ND | 15E | 5260.0 - 5320.0 | 0.013 | ||
| CC ND | 15E | 5500.0 - 5720.0 | 0.013 | ||
| CC | 15E | 5745.0 - 5825.0 | 0.013 |
| Class II Permissive Change to allow portable configuration in the Stryker Medical Bed Procuity (Model 3009) and disabled BT transmitter. Approved for collocation with FCCID: FCCID: QOQW32I. Output power listed is conducted. This grant is valid only when the module is sold to OEM integrators and must be installed by the OEM or OEM integrators. The antenna's as listed in this application must be installed 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. End-users may not be provided with the module installation instructions. OEM integrators and end-users must be provided with transmitter operating conditions for satisfying RF exposure compliance. This device has 20/40/80 MHz bandwidth modes. The 80 MHz mode is limited to channel at 5210MHz, 5290 MHz, 5530 MHz, 5610 MHz and 5775 MHz. The highest reported extremity SAR condition in this filing is 0.17 W/kg(10g). |
| 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 X0KspFn6IzM5PFPlzUU2BA==
| 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: 09/03/2020 Application Dated: 08/26/2020 |
| 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-SDMACP |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Unlicensed National Information Infrastructure TX |
| Notes: | Embedded Wireless module |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15E | 5180.0 - 5240.0 | 0.013 | ||
| CC ND | 15E | 5260.0 - 5320.0 | 0.013 | ||
| CC ND | 15E | 5500.0 - 5720.0 | 0.013 | ||
| CC | 15E | 5745.0 - 5825.0 | 0.013 |
| Class II Permissive Change to allow portable configuration in the Stryker Medical Bed Procuity (Model 3009) and disabled BT transmitter. Approved for collocation with FCCID: FCCID: QOQW32I. Output power listed is conducted. This grant is valid only when the module is sold to OEM integrators and must be installed by the OEM or OEM integrators. The antenna's as listed in this application must be installed 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. End-users may not be provided with the module installation instructions. OEM integrators and end-users must be provided with transmitter operating conditions for satisfying RF exposure compliance. This device has 20/40/80 MHz bandwidth modes. The 80 MHz mode is limited to channel at 5210MHz, 5290 MHz, 5530 MHz, 5610 MHz and 5775 MHz. The highest reported extremity SAR condition in this filing is 0.17 W/kg(10g). |
| 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: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 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: 10/29/2019 Application Dated: 10/29/2019 |
| 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-SDMACP |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Unlicensed National Information Infrastructure TX |
| Notes: | Embedded wireless module |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15E | 5180.0 - 5240.0 | 0.013 | ||
| CC ND | 15E | 5260.0 - 5320.0 | 0.013 | ||
| CC ND | 15E | 5500.0 - 5700.0 | 0.013 | ||
| CC | 15E | 5745.0 - 5825.0 | 0.013 |
| Change of ID from FCC ID: N6C-PMACS Output power listed is conducted. This grant is valid only when the module is sold to OEM integrators and must be installed by the OEM or OEM integrators. The antenna's as listed in this application must be installed 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. End-users may not be provided with the module installation instructions. OEM integrators and end-users must be provided with transmitter operating conditions for satisfying RF exposure compliance. This device has 20/40/80 MHz bandwidth modes. The 80 MHz mode is limited to channel at 5210MHz, 5290 MHz, 5530 MHz, 5610 MHz and 5775 MHz. |
| 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 uKtYMY/gpdlVc/wpBtRM4Q==
| 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: 10/29/2019 Application Dated: 10/29/2019 |
| 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-SDMACP |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Unlicensed National Information Infrastructure TX |
| Notes: | Embedded wireless module |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15E | 5180.0 - 5240.0 | 0.013 | ||
| CC ND | 15E | 5260.0 - 5320.0 | 0.013 | ||
| CC ND | 15E | 5500.0 - 5700.0 | 0.013 | ||
| CC | 15E | 5745.0 - 5825.0 | 0.013 |
| Change of ID from FCC ID: N6C-PMACS Output power listed is conducted. This grant is valid only when the module is sold to OEM integrators and must be installed by the OEM or OEM integrators. The antenna's as listed in this application must be installed 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. End-users may not be provided with the module installation instructions. OEM integrators and end-users must be provided with transmitter operating conditions for satisfying RF exposure compliance. This device has 20/40/80 MHz bandwidth modes. The 80 MHz mode is limited to channel at 5210MHz, 5290 MHz, 5530 MHz, 5610 MHz and 5775 MHz. |
| 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: | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 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: 10/29/2019 Application Dated: 10/29/2019 |
| 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-SDMACP |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Part 15 Spread Spectrum Transmitter |
| Notes: | Embedded wireless module |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15C | 2402.0 - 2480.0 | 0.0016 |
| Change of ID from FCC ID: N6C-PMACS Output power listed is conducted. This grant is valid only when the module is sold to OEM integrators and must be installed by the OEM or OEM integrators. The antenna's as listed in this application must be installed 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. End-users may not be provided with the module installation instructions. OEM integrators and end-users must be provided with transmitter operating conditions for satisfying RF exposure compliance. This device has 20/40 MHz bandwidth modes. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
EAS Grant - Application uJUqUwP7JGq4gWUSNGhUlQ==
| 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: 10/29/2019 Application Dated: 10/29/2019 |
| 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-SDMACP |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Part 15 Spread Spectrum Transmitter |
| Notes: | Embedded wireless module |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15C | 2402.0 - 2480.0 | 0.0016 |
| Change of ID from FCC ID: N6C-PMACS Output power listed is conducted. This grant is valid only when the module is sold to OEM integrators and must be installed by the OEM or OEM integrators. The antenna's as listed in this application must be installed 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. End-users may not be provided with the module installation instructions. OEM integrators and end-users must be provided with transmitter operating conditions for satisfying RF exposure compliance. This device has 20/40 MHz bandwidth modes. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
| 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: 10/29/2019 Application Dated: 10/29/2019 |
| 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-SDMACP |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Digital Transmission System |
| Notes: | Embedded wireless module |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15C | 2402.0 - 2480.0 | 0.0016 | ||
| CC | 15C | 2412.0 - 2462.0 | 0.2 |
| Change of ID from FCC ID: N6C-PMACS Output power listed is conducted. This grant is valid only when the module is sold to OEM integrators and must be installed by the OEM or OEM integrators. The antenna's as listed in this application must be installed 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. End-users may not be provided with the module installation instructions. OEM integrators and end-users must be provided with transmitter operating conditions for satisfying RF exposure compliance. This device has 20/40 MHz bandwidth modes. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
EAS Grant - Application oTxKQu8e7lwjKKLs4xDq/Q==
| 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: 10/29/2019 Application Dated: 10/29/2019 |
| 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-SDMACP |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Digital Transmission System |
| Notes: | Embedded wireless module |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15C | 2402.0 - 2480.0 | 0.0016 | ||
| CC | 15C | 2412.0 - 2462.0 | 0.2 |
| Change of ID from FCC ID: N6C-PMACS Output power listed is conducted. This grant is valid only when the module is sold to OEM integrators and must be installed by the OEM or OEM integrators. The antenna's as listed in this application must be installed 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. End-users may not be provided with the module installation instructions. OEM integrators and end-users must be provided with transmitter operating conditions for satisfying RF exposure compliance. This device has 20/40 MHz bandwidth modes. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
| Mail To: | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| TCB | GRANT OF EQUIPMENT AUTHORIZATION |
TCB |
| Certification | ||
| Issued Under the Authority of the | ||
| Federal Communications Commission | ||
| By: |
|
UL Verification Services Inc. 47173 Benicia Street Fremont, CA 94538 |
Date of Grant: 08/27/2025 Application Dated: 08/27/2025 |
| 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: | Z7A-SDMACP |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Unlicensed National Information Infrastructure TX |
| Notes: | Embedded Wireless module |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15E | 5180.0 - 5240.0 | 0.013 | ||
| CC ND | 15E | 5260.0 - 5320.0 | 0.013 | ||
| CC ND | 15E | 5500.0 - 5700.0 | 0.013 | ||
| CC | 15E | 5745.0 - 5825.0 | 0.013 |
| Class II Permissive Change to allow co-located with Blue Tooth device (FCCID: Z7ALBCA1KU1WA) and disabled Blue Tooth transmitter in FCCID: Z7A-SDMACP. Output power listed is conducted. This grant is valid only when the module is sold to OEM integrators and must be installed by the OEM or OEM integrators. The antennas listed in this application must be installed and not be co-located or operated in conjunction with any other antenna or transmitter. End-users may not be provided with the module installation instructions. OEM integrators and end-users must be provided with transmitter operating conditions for satisfying RF exposure compliance. This device has 20/40/80 MHz bandwidth modes. The 80 MHz mode is limited to channel at 5210MHz, 5290 MHz, 5530 MHz, 5610 MHz, and 5775 MHz. |
| 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 kHU9dh/Y71qAz0x3IQAAbQ==
| TCB | GRANT OF EQUIPMENT AUTHORIZATION |
TCB |
| Certification | ||
| Issued Under the Authority of the | ||
| Federal Communications Commission | ||
| By: |
|
UL Verification Services Inc. (formerly UL CCS) 47173 Benicia Street Fremont, CA 94538 |
Date of Grant: 09/15/2021 Application Dated: 09/07/2021 |
| 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-SDMACP |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Digital Transmission System |
| Notes: | Embedded 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 | 0.2 |
| Class II Permissive Change to allow portable configuration in Stryker Medical Ambulance Cot Power-PRO 2(Model 650700000000, 650705550001, 650705550002, and 650705550003), and disable BT transmitter. Output power listed is conducted. This grant is valid only when the module is sold to OEM integrators and must be installed by the OEM or OEM integrators. The antenna's as listed in this application must be installed and not be co-located or operating in conjunction with any other antenna or transmitter. End-users may not be provided with the module installation instructions. OEM integrators and end-users must be provided with transmitter operating conditions for satisfying RF exposure compliance. This device has 20/40 MHz bandwidth modes. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
EAS Grant - Application kHU9dh/Y71qAz0x3IQAAbQ==
| 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: 09/15/2021 Application Dated: 09/07/2021 |
| 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-SDMACP |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Digital Transmission System |
| Notes: | Embedded 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 | 0.2 |
| Class II Permissive Change to allow portable configuration in Stryker Medical Ambulance Cot Power-PRO 2(Model 650700000000, 650705550001, 650705550002, and 650705550003), and disable BT transmitter. Output power listed is conducted. This grant is valid only when the module is sold to OEM integrators and must be installed by the OEM or OEM integrators. The antenna's as listed in this application must be installed and not be co-located or operating in conjunction with any other antenna or transmitter. End-users may not be provided with the module installation instructions. OEM integrators and end-users must be provided with transmitter operating conditions for satisfying RF exposure compliance. This device has 20/40 MHz bandwidth modes. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
| Mail To: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| TCB | GRANT OF EQUIPMENT AUTHORIZATION |
TCB |
| Certification | ||
| Issued Under the Authority of the | ||
| Federal Communications Commission | ||
| By: |
|
UL Verification Services Inc. 47173 Benicia Street Fremont, CA 94538 |
Date of Grant: 08/27/2025 Application Dated: 08/27/2025 |
| 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: | Z7A-SDMACP |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Digital Transmission System |
| Notes: | Embedded Wireless module |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15C | 2412.0 - 2462.0 | 0.2 |
| Class II Permissive Change to allow co-located with Blue Tooth device (FCCID: Z7ALBCA1KU1WA) and disabled Blue Tooth transmitter in FCCID: Z7A-SDMACP. Output power listed is conducted. This grant is valid only when the module is sold to OEM integrators and must be installed by the OEM or OEM integrators. The antennas listed in this application must be installed and not be co-located or operated in conjunction with any other antenna or transmitter. End-users may not be provided with the module installation instructions. OEM integrators and end-users must be provided with transmitter operating conditions for satisfying RF exposure compliance. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
TCB Grant - Application ej2plmNkD9YY5EYichl/zQ==
| TCB | GRANT OF EQUIPMENT AUTHORIZATION |
TCB |
| Certification | ||
| Issued Under the Authority of the | ||
| Federal Communications Commission | ||
| By: |
|
UL Verification Services Inc. (formerly UL CCS) 47173 Benicia Street Fremont, CA 94538 |
Date of Grant: 09/15/2021 Application Dated: 09/07/2021 |
| 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-SDMACP |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Unlicensed National Information Infrastructure TX |
| Notes: | Embedded Wireless module |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15E | 5180.0 - 5240.0 | 0.013 | ||
| CC ND | 15E | 5260.0 - 5320.0 | 0.013 | ||
| CC ND | 15E | 5500.0 - 5700.0 | 0.013 | ||
| CC | 15E | 5745.0 - 5825.0 | 0.013 |
| Class II Permissive Change to allow portable configuration in Stryker Medical Ambulance Cot Power-PRO 2(Model 650700000000, 650705550001, 650705550002, and 650705550003), and disable BT transmitter. Output power listed is conducted. This grant is valid only when the module is sold to OEM integrators and must be installed by the OEM or OEM integrators. The antenna's as listed in this application must be installed and not be co-located or operating in conjunction with any other antenna or transmitter. End-users may not be provided with the module installation instructions. OEM integrators and end-users must be provided with transmitter operating conditions for satisfying RF exposure compliance. This device has 20/40/80 MHz bandwidth modes. The 80 MHz mode is limited to channel at 5210MHz, 5290 MHz, 5530 MHz, 5610 MHz, and 5775 MHz. |
| 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 ej2plmNkD9YY5EYichl/zQ==
| 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: 09/15/2021 Application Dated: 09/07/2021 |
| 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-SDMACP |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Unlicensed National Information Infrastructure TX |
| Notes: | Embedded Wireless module |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15E | 5180.0 - 5240.0 | 0.013 | ||
| CC ND | 15E | 5260.0 - 5320.0 | 0.013 | ||
| CC ND | 15E | 5500.0 - 5700.0 | 0.013 | ||
| CC | 15E | 5745.0 - 5825.0 | 0.013 |
| Class II Permissive Change to allow portable configuration in Stryker Medical Ambulance Cot Power-PRO 2(Model 650700000000, 650705550001, 650705550002, and 650705550003), and disable BT transmitter. Output power listed is conducted. This grant is valid only when the module is sold to OEM integrators and must be installed by the OEM or OEM integrators. The antenna's as listed in this application must be installed and not be co-located or operating in conjunction with any other antenna or transmitter. End-users may not be provided with the module installation instructions. OEM integrators and end-users must be provided with transmitter operating conditions for satisfying RF exposure compliance. This device has 20/40/80 MHz bandwidth modes. The 80 MHz mode is limited to channel at 5210MHz, 5290 MHz, 5530 MHz, 5610 MHz, and 5775 MHz. |
| 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: | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| TCB | GRANT OF EQUIPMENT AUTHORIZATION |
TCB |
| Certification | ||
| Issued Under the Authority of the | ||
| Federal Communications Commission | ||
| By: |
|
UL Verification Services Inc. (formerly UL CCS) 47173 Benicia Street Fremont, CA 94538 |
Date of Grant: 09/03/2020 Application Dated: 08/26/2020 |
| 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-SDMACP |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Digital Transmission System |
| Notes: | Embedded Wireless module |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15C | 2402.0 - 2480.0 | 0.2 |
| Class II Permissive Change to allow portable configuration in the Stryker Medical Bed Procuity (Model 3009) and disable BT transmitter. Approved for collocation with FCCID: FCCID: QOQW32I. Output power listed is conducted. This grant is valid only when the module is sold to OEM integrators and must be installed by the OEM or OEM integrators. The antenna's as listed in this application must be installed 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. End-users may not be provided with the module installation instructions. OEM integrators and end-users must be provided with transmitter operating conditions for satisfying RF exposure compliance. This device has 20/40 MHz bandwidth modes. The highest reported extremity SAR condition in this filing is 0.80 W/kg(10g). |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
EAS Grant - Application 8Hc2mfPGSkINDqO1WeS9Dg==
| 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: 09/03/2020 Application Dated: 08/26/2020 |
| 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-SDMACP |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Digital Transmission System |
| Notes: | Embedded Wireless module |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15C | 2402.0 - 2480.0 | 0.2 |
| Class II Permissive Change to allow portable configuration in the Stryker Medical Bed Procuity (Model 3009) and disable BT transmitter. Approved for collocation with FCCID: FCCID: QOQW32I. Output power listed is conducted. This grant is valid only when the module is sold to OEM integrators and must be installed by the OEM or OEM integrators. The antenna's as listed in this application must be installed 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. End-users may not be provided with the module installation instructions. OEM integrators and end-users must be provided with transmitter operating conditions for satisfying RF exposure compliance. This device has 20/40 MHz bandwidth modes. The highest reported extremity SAR condition in this filing is 0.80 W/kg(10g). |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
| Mail To: |