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 ID | Z7A-SDMAN |
|---|---|
| Mirrors | fcc.id | gov | fccid.ai |
| Grantee Code | Z7A |
| Product Code | SDMAN |
| Applicant Business | Stryker Medical 🇺🇸 |
| Related Domains | |
| Equipment Class | SDIO Wireless Module |
| Test Firm | Bureau Veritas Consumer Products Services, Inc. |
Operating Frequencies
| Frequency Range | Application Purpose | Final Action Date |
|---|---|---|
| 5180-5240 MHz | Class II permissive change or modification of presently authorized equipment | 2016-04-12 |
| 2412-2462 MHz | Class II permissive change or modification of presently authorized equipment | 2016-04-12 |
| 2402-2480 MHz | Change in identification of presently authorized equipment. Original FCC ID: N6C-SDMAN Grant Date: 09/14/2015 | 2016-03-24 |
| 5180-5320 MHz | Change in identification of presently authorized equipment. Original FCC ID: N6C-SDMAN Grant Date: 09/14/2015 | 2016-03-24 |
Exhibits
| Document | Type | Available | File |
|---|---|---|---|
| Users Manual | Users Manual | 2016-03-24 | PDF 158 KB |
| Users manual | Users Manual | 2016-03-24 | PDF 158 KB |
| Internal Photos | Internal Photos | 2016-04-12 | PDF 212.5 KB |
| Host External Photos | External Photos | 2016-04-12 | PDF 170 KB |
| External Photos | External Photos | 2016-03-24 | PDF 125.1 KB |
| Label | ID Label/Location Info | 2016-03-24 | PDF 299.6 KB |
| Test Setup Photos | Test Setup Photos | 2016-04-12 | PDF 132.3 KB |
| SAR Test Report | RF Exposure Info | 2016-04-12 | PDF 3.6 MB |
| Test Report | Test Report | 2016-04-12 | PDF 3.6 MB |
| Permissive Change Letter | Cover Letter(s) | 2016-04-12 | PDF 305.5 KB |
| Product Certification Rep Auth Letter | Cover Letter(s) | 2016-04-12 | PDF 349.1 KB |
| Change of ID Request Letter from Orig. Applicant | Cover Letter(s) | 2016-03-24 | PDF 155.7 KB |
| Change of ID request Letter | Cover Letter(s) | 2016-03-24 | PDF 340.7 KB |
Application Information
| Application ID | az1Cd7bfzrmcgEY4AKakew== |
|---|---|
| Final Action Date | 2016-04-12 |
| Application Purpose | Class II permissive change or modification of presently authorized equipment |
| Applicant FRN | 0021243142 |
| Model | SDMAN |
| Frequency Range | 5180-5240 MHz |
| Equipment Class | NII - Unlicensed National Information Infrastructure TX |
| Device Description | SDIO Wireless Module |
| Responsible Party | Michael Hayes, Sr Principle EE, mike.hayes@stryker.com |
| Test Firm | Sarb Shelopal, Bureau Veritas Consumer Products Services, Inc., Sarbjit.Shelopal@bureauveritas.com |
| TCB Email | tcb@siemic.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 | Single Modular Approval |
| 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 | 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. |
Applications
| Application ID | Date | Purpose |
|---|---|---|
| az1Cd7bfzrmcgEY4AKakew== | 2016-04-12 | Class II permissive change or modification of presently authorized equipment |
| RHA5GJlaZ/+c7QvbyF/L7w== | 2016-04-12 | Class II permissive change or modification of presently authorized equipment |
| xzjpy2aMLsPMfXjoU7gT5g== | 2016-03-24 | Change in identification of presently authorized equipment. Original FCC ID: N6C-SDMAN Grant Date: 09/14/2015 |
| EAq5YdMSkk4h/sRuRhEfAQ== | 2016-03-24 | Change in identification of presently authorized equipment. Original FCC ID: N6C-SDMAN Grant Date: 09/14/2015 |
Equipment Authorization
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. |
| 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. |
| 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). |
| 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: |