FCC ID 2AR2I-CSCM6000
CADD Solis
by Smiths Medical ASD, Inc.
Grantee Code: 2AR2I Product Code: CSCM6000
Latest application date: 2019-11-12
FCC ID Device Details
| FCC ID | 2AR2I-CSCM6000 |
|---|---|
| Mirrors | fcc.id | gov | fccid.ai |
| Grantee Code | 2AR2I |
| Product Code | CSCM6000 |
| Applicant Business | Smiths Medical ASD, Inc. 🇺🇸 |
| Related Domains | |
| Equipment Class | CADD Solis |
| Test Firm | UL Japan, Inc. Head office EMC Lab. |
Operating Frequencies
| Frequency Range | Application Purpose | Final Action Date |
|---|---|---|
| 2402-2480 MHz | Class II permissive change or modification of presently authorized equipment | 2019-11-12 |
| 5180-5320 MHz | Class II permissive change or modification of presently authorized equipment | 2019-11-12 |
| 2402-2480 MHz | Change in identification of presently authorized equipment. Original FCC ID: N6C-SDMAC Grant Date: 11/08/2016 | 2019-10-02 |
| 2402-2480 MHz | Change in identification of presently authorized equipment. Original FCC ID: N6C-SDMAC Grant Date: 11/08/2016 | 2019-10-02 |
| 5180-5320 MHz | Change in identification of presently authorized equipment. Original FCC ID: N6C-SDMAC Grant Date: 11/08/2016 | 2019-10-02 |
Exhibits
| Document | Type | Available | File |
|---|---|---|---|
| User Manual | Users Manual | 2019-11-12 | PDF 4.8 MB |
| User Manual part 1 of 2 | Users Manual | 2019-11-12 | PDF 3.5 MB |
| User Manual part 2 of 2 | Users Manual | 2019-11-12 | PDF 3.5 MB |
| Internal Photos | Internal Photos | 2019-11-12 | PDF 292.2 KB |
| Internal Photos | Internal Photos | 2019-10-02 | PDF 223.4 KB |
| External Photos | External Photos | 2019-11-12 | PDF 292.2 KB |
| External Photos | External Photos | 2019-10-02 | PDF 223.4 KB |
| ID Label | ID Label/Location Info | 2019-11-12 | PDF 33 KB |
| ID Label | ID Label/Location Info | 2019-10-02 | PDF 33 KB |
| Test Setup Photos | Test Setup Photos | 2019-11-12 | PDF 380.3 KB |
| Agent Authorization Letter | Cover Letter(s) | 2019-11-12 | PDF 26.6 KB |
| Cover Letter | Cover Letter(s) | 2019-11-12 | PDF 22 KB |
| Cover Letter | Cover Letter(s) | 2019-10-02 | PDF 389.8 KB |
| SAR report part 1 of 2 | RF Exposure Info | 2019-11-12 | PDF 3.3 MB |
| SAR report part 2 of 2 | RF Exposure Info | 2019-11-12 | PDF 2.9 MB |
Application Information
| Application ID | wB3IT0hyVULkSHlCsy0c6g== |
|---|---|
| Final Action Date | 2019-11-12 |
| Application Purpose | Class II permissive change or modification of presently authorized equipment |
| Applicant FRN | 0028060820 |
| Model | CSCM6000 |
| Frequency Range | 2402-2480 MHz |
| Equipment Class | DTS - Digital Transmission System |
| Device Description | CADD Solis |
| Responsible Party | Maxine Chen, Maxine.Chen@smiths-medical.com |
| Agent | Toshiro Toshiro Toshiro, Silex, kometani@silex.jp |
| Test Firm | Tetsuya Hashimoto, UL Japan, Inc. Head office EMC Lab., Tetsuya.Hashimoto@jp.ul.com |
| TCB Email | greg.kiemel@element.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 | Single Modular Approval. Output power listed is Conducted (Peak). For professional installation only. Device shall not be sold to general public. This device has a 20 MHz and 40 MHz bandwidth mode. 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. This C2PC is to authorize a specific portable exposure condition that results when this module is installed in the Smiths Medical, Model CADD Solis ambulatory infusion pump. Bluetooth is disabled in this configuration. The highest reported SAR value is 0.61 W/kg. |
Applications
| Application ID | Date | Purpose |
|---|---|---|
| wB3IT0hyVULkSHlCsy0c6g== | 2019-11-12 | Class II permissive change or modification of presently authorized equipment |
| 2Gt875GZFqAGBZcMGS1n6g== | 2019-11-12 | Class II permissive change or modification of presently authorized equipment |
| eI/JC8FvWl5ZEwwnY03WRA== | 2019-10-02 | Change in identification of presently authorized equipment. Original FCC ID: N6C-SDMAC Grant Date: 11/08/2016 |
| dU1p2JtW88TJAUa+Ol9rdg== | 2019-10-02 | Change in identification of presently authorized equipment. Original FCC ID: N6C-SDMAC Grant Date: 11/08/2016 |
| TMg9rjqdbeIzdxjvp/TyaQ== | 2019-10-02 | Change in identification of presently authorized equipment. Original FCC ID: N6C-SDMAC Grant Date: 11/08/2016 |
Equipment Authorization
Grants
TCB Grant - Application wB3IT0hyVULkSHlCsy0c6g==
| TCB | GRANT OF EQUIPMENT AUTHORIZATION |
TCB |
| Certification | ||
| Issued Under the Authority of the | ||
| Federal Communications Commission | ||
| By: |
|
Element Materials Technology Portland - Evergreen 6775 NE Evergreen Parkway, Suite 400 Hillsboro, OR 97124 |
Date of Grant: 11/12/2019 Application Dated: 11/12/2019 |
| Smiths Medical ASD, Inc. |
| 6000 Nathan Lane North |
| Plymouth, MN 55442 |
| Attention: Maxine Chen |
| 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: | 2AR2I-CSCM6000 |
| Name of Grantee: | Smiths Medical ASD, Inc. |
| Equipment Class: | Digital Transmission System |
| Notes: | CADD Solis |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15C | 2412.0 - 2462.0 | 0.2999 | ||
| CC | 15C | 2402.0 - 2480.0 | 0.0016 |
| Single Modular Approval. Output power listed is Conducted (Peak). For professional installation only. Device shall not be sold to general public. This device has a 20 MHz and 40 MHz bandwidth mode. 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. This C2PC is to authorize a specific portable exposure condition that results when this module is installed in the Smiths Medical, Model CADD Solis ambulatory infusion pump. Bluetooth is disabled in this configuration. The highest reported SAR value is 0.61 W/kg. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
EAS Grant - Application wB3IT0hyVULkSHlCsy0c6g==
| COPY |
FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION |
COPY |
| Certification |
|
Smiths Medical ASD, Inc. 6000 Nathan Lane North Plymouth, MN 55442 United States |
Date of Grant: 11/12/2019 Application Dated: 11/12/2019 |
| Attention: Maxine Chen |
| 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: | 2AR2I-CSCM6000 |
| Name of Grantee: | Smiths Medical ASD, Inc. |
| Equipment Class: | Digital Transmission System |
| Notes: | CADD Solis |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15C | 2412.0 - 2462.0 | 0.2999 | ||
| CC | 15C | 2402.0 - 2480.0 | 0.0016 |
| Single Modular Approval. Output power listed is Conducted (Peak). For professional installation only. Device shall not be sold to general public. This device has a 20 MHz and 40 MHz bandwidth mode. 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. This C2PC is to authorize a specific portable exposure condition that results when this module is installed in the Smiths Medical, Model CADD Solis ambulatory infusion pump. Bluetooth is disabled in this configuration. The highest reported SAR value is 0.61 W/kg. |
| 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: |
|
Element Materials Technology Portland - Evergreen 6775 NE Evergreen Parkway, Suite 400 Hillsboro, OR 97124 |
Date of Grant: 10/02/2019 Application Dated: 10/02/2019 |
| Smiths Medical ASD, Inc. |
| 6000 Nathan Lane North |
| Plymouth, MN 55442 |
| Attention: Maxine Chen |
| 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: | 2AR2I-CSCM6000 |
| Name of Grantee: | Smiths Medical ASD, Inc. |
| Equipment Class: | Unlicensed National Information Infrastructure TX |
| Notes: | CADD Solis |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| 38 CC | 15E | 5180.0 - 5320.0 | 0.0251 | ||
| 38 CC | 15E | 5500.0 - 5700.0 | 0.009 | ||
| 38 CC | 15E | 5745.0 - 5825.0 | 0.0139 |
| Single Modular Approval. Output power listed is Conducted. For professional installation only. Device shall not be sold to general public. This device has a 20 MHz, 40 MHz and 80 MHz bandwidth mode for 5 GHz bands. 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. This device complies with the Dynamic Frequency Selection (DFS) requirements of Report and KDB 905462 D01 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. |
EAS Grant - Application TMg9rjqdbeIzdxjvp/TyaQ==
| COPY |
FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION |
COPY |
| Certification |
|
Smiths Medical ASD, Inc. 6000 Nathan Lane North Plymouth, MN 55442 United States |
Date of Grant: 10/02/2019 Application Dated: 10/02/2019 |
| Attention: Maxine Chen |
| 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: | 2AR2I-CSCM6000 |
| Name of Grantee: | Smiths Medical ASD, Inc. |
| Equipment Class: | Unlicensed National Information Infrastructure TX |
| Notes: | CADD Solis |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| 38 CC | 15E | 5180.0 - 5320.0 | 0.0251 | ||
| 38 CC | 15E | 5500.0 - 5700.0 | 0.009 | ||
| 38 CC | 15E | 5745.0 - 5825.0 | 0.0139 |
| Single Modular Approval. Output power listed is Conducted. For professional installation only. Device shall not be sold to general public. This device has a 20 MHz, 40 MHz and 80 MHz bandwidth mode for 5 GHz bands. 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. This device complies with the Dynamic Frequency Selection (DFS) requirements of Report and KDB 905462 D01 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. |
| Mail To: | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| TCB | GRANT OF EQUIPMENT AUTHORIZATION |
TCB |
| Certification | ||
| Issued Under the Authority of the | ||
| Federal Communications Commission | ||
| By: |
|
Element Materials Technology Portland - Evergreen 6775 NE Evergreen Parkway, Suite 400 Hillsboro, OR 97124 |
Date of Grant: 10/02/2019 Application Dated: 10/02/2019 |
| Smiths Medical ASD, Inc. |
| 6000 Nathan Lane North |
| Plymouth, MN 55442 |
| Attention: Maxine Chen |
| 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: | 2AR2I-CSCM6000 |
| Name of Grantee: | Smiths Medical ASD, Inc. |
| Equipment Class: | Digital Transmission System |
| Notes: | CADD Solis |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15C | 2412.0 - 2462.0 | 0.2999 | ||
| CC | 15C | 2402.0 - 2480.0 | 0.0016 |
| Single Modular Approval. Output power listed is Conducted( Peak). For professional installation only. Device shall not be sold to general public. This device has a 20 MHz and 40 MHz bandwidth mode. 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. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
EAS Grant - Application eI/JC8FvWl5ZEwwnY03WRA==
| COPY |
FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION |
COPY |
| Certification |
|
Smiths Medical ASD, Inc. 6000 Nathan Lane North Plymouth, MN 55442 United States |
Date of Grant: 10/02/2019 Application Dated: 10/02/2019 |
| Attention: Maxine Chen |
| 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: | 2AR2I-CSCM6000 |
| Name of Grantee: | Smiths Medical ASD, Inc. |
| Equipment Class: | Digital Transmission System |
| Notes: | CADD Solis |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15C | 2412.0 - 2462.0 | 0.2999 | ||
| CC | 15C | 2402.0 - 2480.0 | 0.0016 |
| Single Modular Approval. Output power listed is Conducted( Peak). For professional installation only. Device shall not be sold to general public. This device has a 20 MHz and 40 MHz bandwidth mode. 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. |
| 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: |
|
Element Materials Technology Portland - Evergreen 6775 NE Evergreen Parkway, Suite 400 Hillsboro, OR 97124 |
Date of Grant: 10/02/2019 Application Dated: 10/02/2019 |
| Smiths Medical ASD, Inc. |
| 6000 Nathan Lane North |
| Plymouth, MN 55442 |
| Attention: Maxine Chen |
| 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: | 2AR2I-CSCM6000 |
| Name of Grantee: | Smiths Medical ASD, Inc. |
| Equipment Class: | Part 15 Spread Spectrum Transmitter |
| Notes: | CADD Solis |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15C | 2402.0 - 2480.0 | 0.0014 |
| Single Modular Approval. Output power listed is Conducted(Peak). For professional installation only. Device shall not be sold to general public. 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. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
EAS Grant - Application dU1p2JtW88TJAUa+Ol9rdg==
| COPY |
FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION |
COPY |
| Certification |
|
Smiths Medical ASD, Inc. 6000 Nathan Lane North Plymouth, MN 55442 United States |
Date of Grant: 10/02/2019 Application Dated: 10/02/2019 |
| Attention: Maxine Chen |
| 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: | 2AR2I-CSCM6000 |
| Name of Grantee: | Smiths Medical ASD, Inc. |
| Equipment Class: | Part 15 Spread Spectrum Transmitter |
| Notes: | CADD Solis |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15C | 2402.0 - 2480.0 | 0.0014 |
| Single Modular Approval. Output power listed is Conducted(Peak). For professional installation only. Device shall not be sold to general public. 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. |
| 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: |
|
Element Materials Technology Portland - Evergreen 6775 NE Evergreen Parkway, Suite 400 Hillsboro, OR 97124 |
Date of Grant: 11/12/2019 Application Dated: 11/12/2019 |
| Smiths Medical ASD, Inc. |
| 6000 Nathan Lane North |
| Plymouth, MN 55442 |
| Attention: Maxine Chen |
| 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: | 2AR2I-CSCM6000 |
| Name of Grantee: | Smiths Medical ASD, Inc. |
| Equipment Class: | Unlicensed National Information Infrastructure TX |
| Notes: | CADD Solis |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| 38 CC | 15E | 5180.0 - 5320.0 | 0.0251 | ||
| 38 CC | 15E | 5500.0 - 5700.0 | 0.009 | ||
| 38 CC | 15E | 5745.0 - 5825.0 | 0.0139 |
| Single Modular Approval. Output power listed is Conducted. For professional installation only. Device shall not be sold to general public. This device has a 20 MHz, 40 MHz and 80 MHz bandwidth mode for 5 GHz bands. 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. This device complies with the Dynamic Frequency Selection (DFS) requirements of Report and KDB 905462 D01 as a Client only without Radar Detection. This C2PC is to authorize a specific portable exposure condition that results when this module is installed in the Smiths Medical, Model CADD Solis ambulatory infusion pump. The highest reported SAR value is 0.13 W/kg. |
| 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. |
EAS Grant - Application 2Gt875GZFqAGBZcMGS1n6g==
| COPY |
FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION |
COPY |
| Certification |
|
Smiths Medical ASD, Inc. 6000 Nathan Lane North Plymouth, MN 55442 United States |
Date of Grant: 11/12/2019 Application Dated: 11/12/2019 |
| Attention: Maxine Chen |
| 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: | 2AR2I-CSCM6000 |
| Name of Grantee: | Smiths Medical ASD, Inc. |
| Equipment Class: | Unlicensed National Information Infrastructure TX |
| Notes: | CADD Solis |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| 38 CC | 15E | 5180.0 - 5320.0 | 0.0251 | ||
| 38 CC | 15E | 5500.0 - 5700.0 | 0.009 | ||
| 38 CC | 15E | 5745.0 - 5825.0 | 0.0139 |
| Single Modular Approval. Output power listed is Conducted. For professional installation only. Device shall not be sold to general public. This device has a 20 MHz, 40 MHz and 80 MHz bandwidth mode for 5 GHz bands. 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. This device complies with the Dynamic Frequency Selection (DFS) requirements of Report and KDB 905462 D01 as a Client only without Radar Detection. This C2PC is to authorize a specific portable exposure condition that results when this module is installed in the Smiths Medical, Model CADD Solis ambulatory infusion pump. The highest reported SAR value is 0.13 W/kg. |
| 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. |
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