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 ID2AR2I-CSCM6000
Mirrorsfcc.id | gov | fccid.ai
Grantee Code2AR2I
Product CodeCSCM6000
Applicant BusinessSmiths Medical ASD, Inc. 🇺🇸
Related Domains smiths-medical.com
Equipment ClassCADD Solis
Test FirmUL Japan, Inc. Head office EMC Lab.

Operating Frequencies

Frequency RangeApplication PurposeFinal Action Date
2402-2480 MHzClass II permissive change or modification of presently authorized equipment2019-11-12
5180-5320 MHzClass II permissive change or modification of presently authorized equipment2019-11-12
2402-2480 MHzChange in identification of presently authorized equipment. Original FCC ID: N6C-SDMAC Grant Date: 11/08/20162019-10-02
2402-2480 MHzChange in identification of presently authorized equipment. Original FCC ID: N6C-SDMAC Grant Date: 11/08/20162019-10-02
5180-5320 MHzChange in identification of presently authorized equipment. Original FCC ID: N6C-SDMAC Grant Date: 11/08/20162019-10-02

Exhibits

DocumentTypeAvailableFile
User ManualUsers Manual2019-11-12PDF 4.8 MB
User Manual part 1 of 2Users Manual2019-11-12PDF 3.5 MB
User Manual part 2 of 2Users Manual2019-11-12PDF 3.5 MB
Internal PhotosInternal Photos2019-11-12PDF 292.2 KB
Internal PhotosInternal Photos2019-10-02PDF 223.4 KB
External PhotosExternal Photos2019-11-12PDF 292.2 KB
External PhotosExternal Photos2019-10-02PDF 223.4 KB
ID LabelID Label/Location Info2019-11-12PDF 33 KB
ID LabelID Label/Location Info2019-10-02PDF 33 KB
Test Setup PhotosTest Setup Photos2019-11-12PDF 380.3 KB
Agent Authorization LetterCover Letter(s)2019-11-12PDF 26.6 KB
Cover LetterCover Letter(s)2019-11-12PDF 22 KB
Cover LetterCover Letter(s)2019-10-02PDF 389.8 KB
SAR report part 1 of 2RF Exposure Info2019-11-12PDF 3.3 MB
SAR report part 2 of 2RF Exposure Info2019-11-12PDF 2.9 MB

Application Information

Application IDwB3IT0hyVULkSHlCsy0c6g==
Final Action Date2019-11-12
Application PurposeClass II permissive change or modification of presently authorized equipment
Applicant FRN0028060820
ModelCSCM6000
Frequency Range2402-2480 MHz
Equipment ClassDTS - Digital Transmission System
Device DescriptionCADD Solis
Responsible PartyMaxine Chen, Maxine.Chen@smiths-medical.com , 7633833439
AgentToshiro Toshiro Toshiro, Silex, kometani@silex.jp
Test FirmTetsuya Hashimoto, UL Japan, Inc. Head office EMC Lab., Tetsuya.Hashimoto@jp.ul.com , +81-596-24-8116
TCB Emailgreg.kiemel@element.com
TCB ScopeA4: UNII devices & low power transmitters using spread spectrum techniques
Short-Term ConfidentialityNo
Long-Term ConfidentialityNo
Grant DeferralNo
Modular EquipmentSingle Modular Approval
Composite DeviceYes
Composite PartNo
Cognitive RadioNo
Authorization WaiverNo
Authorization Waiver ApprovedNo
Section 5301 CertificationYes
Related OET Knowledge DataBase InquiryNo
Grant CommentsSingle 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 IDDatePurpose
wB3IT0hyVULkSHlCsy0c6g==2019-11-12Class II permissive change or modification of presently authorized equipment
2Gt875GZFqAGBZcMGS1n6g==2019-11-12Class II permissive change or modification of presently authorized equipment
eI/JC8FvWl5ZEwwnY03WRA==2019-10-02Change in identification of presently authorized equipment. Original FCC ID: N6C-SDMAC Grant Date: 11/08/2016
dU1p2JtW88TJAUa+Ol9rdg==2019-10-02Change in identification of presently authorized equipment. Original FCC ID: N6C-SDMAC Grant Date: 11/08/2016
TMg9rjqdbeIzdxjvp/TyaQ==2019-10-02Change in identification of presently authorized equipment. Original FCC ID: N6C-SDMAC Grant Date: 11/08/2016

Equipment Authorization

FrequencyOutputRulesGrant Notes
2402-2480 MHz0.001400015CCC
2402-2480 MHz0.001615CCC
2412-2462 MHz0.299915CCC
5180-5320 MHz0.025115E38, CC
5500-5700 MHz0.00915E38, CC
5745-5825 MHz0.013915E38, CC

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.

TCB Grant - Application TMg9rjqdbeIzdxjvp/TyaQ==

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.

TCB Grant - Application eI/JC8FvWl5ZEwwnY03WRA==

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.

TCB Grant - Application dU1p2JtW88TJAUa+Ol9rdg==

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.

TCB Grant - Application 2Gt875GZFqAGBZcMGS1n6g==

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.

Mail To: