FCC ID VO9-CCPROII
blood measuring instrument
by Roche Diagnostics GmbH
Grantee Code: VO9 Product Code: CCPROII
Latest application date: 2023-07-14
FCC ID Device Details
Operating Frequencies
| Frequency Range | Application Purpose | Final Action Date |
|---|---|---|
| 2412-2462 MHz | Original Equipment | 2023-07-14 |
| 5180-5240 MHz | Original Equipment | 2023-07-14 |
Exhibits
| Document | Type | Available | File |
|---|---|---|---|
| User Manual - English | Users Manual | 2023-07-14 | PDF 4.3 MB |
| User manual | Users Manual | 2023-07-14 | PDF 4.3 MB |
| Internal photos | Internal Photos | 2023-07-14 | PDF 1.8 MB |
| External photos | External Photos | 2023-07-14 | PDF 492.3 KB |
| Label | ID Label/Location Info | 2023-07-14 | PDF 24.8 KB |
| SAR Test Report- Test Setup Photos | RF Exposure Info | 2023-07-14 | PDF 1.1 MB |
| Test Setup Photos | Test Setup Photos | 2023-07-14 | PDF 750.6 KB |
| Test setup photos | Test Setup Photos | 2023-07-14 | PDF 750.6 KB |
| SAR Test Report - Caldata | RF Exposure Info | 2023-07-14 | PDF 2.6 MB |
| SAR Test Report - Main Report | RF Exposure Info | 2023-07-14 | PDF 1.9 MB |
| Test Report DTS - WLAN 2.4 GHz Annex Part 1 | Test Report | 2023-07-14 | PDF 5.4 MB |
| Test Report DTS - WLAN 2.4 GHz Annex Part 2 | Test Report | 2023-07-14 | PDF 4.1 MB |
| Test Report DTS - WLAN 2.4 GHz Main Report | Test Report | 2023-07-14 | PDF 2.9 MB |
| Test Report NII - WLAN 5 GHz Annex Part 1 | Test Report | 2023-07-14 | PDF 5.3 MB |
| Test Report NII - WLAN 5 GHz Annex Part 2 | Test Report | 2023-07-14 | PDF 5.5 MB |
| Test Report NII - WLAN 5 GHz Annex Part 3 | Test Report | 2023-07-14 | PDF 5.4 MB |
| Test Report NII - WLAN 5 GHz Annex Part 4 | Test Report | 2023-07-14 | PDF 364.2 KB |
| Test Report NII - WLAN 5 GHz Main Report | Test Report | 2023-07-14 | PDF 3.4 MB |
| 2.911(d)(5) letter | Attestation Statements | 2023-07-14 | PDF 467.6 KB |
| 2.911(d)(7) letter | Attestation Statements | 2023-07-14 | PDF 281.1 KB |
| LTC | Cover Letter(s) | 2023-07-14 | PDF 226.7 KB |
| Block diagram Metadata only | Block Diagram | PDF 368.5 KB | |
| Schematics - BOM Metadata only | Schematics | PDF 107.2 KB | |
| Schematics - Curcuit Diagram Metadata only | Schematics | PDF 571.1 KB | |
| Schematics - Module Metadata only | Schematics | PDF 758.9 KB | |
| Schematics - PCB Layout Metadata only | Schematics | PDF 3.3 MB | |
| Operational Description - Datasheet Metadata only | Operational Description | PDF 570.2 KB | |
| Operational Description - Software Security Metadata only | Operational Description | PDF 245 KB | |
| Operational Description - U-NII Declaration Letter Metadata only | Operational Description | PDF 62.4 KB |
Application Information
| Application ID | xQZgd/6O51YCgC7tjBhuwQ== |
|---|---|
| Final Action Date | 2023-07-14 |
| Application Purpose | Original Equipment |
| Applicant FRN | 0016954943 |
| Model | CCPROII |
| Frequency Range | 2412-2462 MHz |
| Equipment Class | DTS - Digital Transmission System |
| Device Description | blood measuring instrument |
| Responsible Party | Christian Paulus, christian.paulus@roche.com  , +49621759 |
| Test Firm | Gerald Schmidt, CTC advanced GmbH, mail@ctcadvanced.com  , 49-681-598-0 |
| TCB Email | tcb@ctcadvanced.com |
| TCB Scope | A4: UNII devices & low power transmitters using spread spectrum techniques |
| Short-Term Confidentiality | No |
| Long-Term Confidentiality | Yes |
| 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 | Output power listed is peak conducted. This device supports IEEE 802.11b (Wi-Fi 1) with a 20 MHz bandwidth mode, IEEE 802.11g (Wi-Fi 3) with a 20 MHz bandwidth mode and IEEE 802.11n (Wi-Fi 5) with a 20 MHz, 40 MHz bandwidth mode. For body worn and extremities operation this device has been tested touched to the phantom and meets FCC RF exposure guidelines. The highest reported SAR for body-worn and extremities SAR exposure conditions are 0.06 W/kg and 0.03 W/kg, respectively. |
Applications
| Application ID | Date | Purpose |
|---|---|---|
| xQZgd/6O51YCgC7tjBhuwQ== | 2023-07-14 | Original Equipment |
| 2ORkgcqlTw9D5E1FrW8F6A== | 2023-07-14 | Original Equipment |
Equipment Authorization
Grants
TCB Grant - Application xQZgd/6O51YCgC7tjBhuwQ==
| TCB | GRANT OF EQUIPMENT AUTHORIZATION |
TCB |
| Certification | ||
| Issued Under the Authority of the | ||
| Federal Communications Commission | ||
| By: |
|
CTC advanced GmbH Untertuerkheimer Strasse 6-10 66117 Saarbruecken, Germany |
Date of Grant: 07/14/2023 Application Dated: 07/14/2023 |
| Roche Diagnostics GmbH |
| Sandhofer Strasse 116 |
| Mannheim, 68305 Germany |
| Attention: Christian Paulus |
| 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: | VO9-CCPROII |
| Name of Grantee: | Roche Diagnostics GmbH |
| Equipment Class: | Digital Transmission System |
| Notes: | blood measuring instrument |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15C | 2412.0 - 2462.0 | 0.19055 |
| Output power listed is peak conducted. This device supports IEEE 802.11b (Wi-Fi 1) with a 20 MHz bandwidth mode, IEEE 802.11g (Wi-Fi 3) with a 20 MHz bandwidth mode and IEEE 802.11n (Wi-Fi 5) with a 20 MHz, 40 MHz bandwidth mode. For body worn and extremities operation this device has been tested touched to the phantom and meets FCC RF exposure guidelines. The highest reported SAR for body-worn and extremities SAR exposure conditions are 0.06 W/kg and 0.03 W/kg, respectively. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
EAS Grant - Application xQZgd/6O51YCgC7tjBhuwQ==
| COPY |
FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION |
COPY |
| Certification |
|
Roche Diagnostics GmbH Sandhofer Strasse 116 Mannheim, 68305 Germany |
Date of Grant: 07/14/2023 Application Dated: 07/14/2023 |
| Attention: Christian Paulus |
| 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: | VO9-CCPROII |
| Name of Grantee: | Roche Diagnostics GmbH |
| Equipment Class: | Digital Transmission System |
| Notes: | blood measuring instrument |
| Modular Type: | Does not apply |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15C | 2412.0 - 2462.0 | 0.19055 |
| Output power listed is peak conducted. This device supports IEEE 802.11b (Wi-Fi 1) with a 20 MHz bandwidth mode, IEEE 802.11g (Wi-Fi 3) with a 20 MHz bandwidth mode and IEEE 802.11n (Wi-Fi 5) with a 20 MHz, 40 MHz bandwidth mode. For body worn and extremities operation this device has been tested touched to the phantom and meets FCC RF exposure guidelines. The highest reported SAR for body-worn and extremities SAR exposure conditions are 0.06 W/kg and 0.03 W/kg, respectively. |
| 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: |
|
CTC advanced GmbH Untertuerkheimer Strasse 6-10 66117 Saarbruecken, Germany |
Date of Grant: 07/14/2023 Application Dated: 07/14/2023 |
| Roche Diagnostics GmbH |
| Sandhofer Strasse 116 |
| Mannheim, 68305 Germany |
| Attention: Christian Paulus |
| 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: | VO9-CCPROII |
| Name of Grantee: | Roche Diagnostics GmbH |
| Equipment Class: | Unlicensed National Information Infrastructure TX |
| Notes: | blood measuring instrument |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15E | 5180.0 - 5240.0 | 0.01905 | ||
| CC | 15E | 5745.0 - 5825.0 | 0.00562 |
| Output power listed is average conducted. This device supports IEEE 802.11a (Wi-Fi 2) with a 20 MHz bandwidth mode and IEEE 802.11n (Wi-Fi 4) with a 20 MHz, 40 MHz bandwidth mode. For body worn and extremities operation this device has been tested touched to the phantom and meets FCC RF exposure guidelines. The highest reported SAR for body-worn and extremities SAR exposure conditions are 0.13 W/kg and 0.04 W/kg, respectively. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
EAS Grant - Application 2ORkgcqlTw9D5E1FrW8F6A==
| COPY |
FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION |
COPY |
| Certification |
|
Roche Diagnostics GmbH Sandhofer Strasse 116 Mannheim, 68305 Germany |
Date of Grant: 07/14/2023 Application Dated: 07/14/2023 |
| Attention: Christian Paulus |
| 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: | VO9-CCPROII |
| Name of Grantee: | Roche Diagnostics GmbH |
| Equipment Class: | Unlicensed National Information Infrastructure TX |
| Notes: | blood measuring instrument |
| Modular Type: | Does not apply |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15E | 5180.0 - 5240.0 | 0.01905 | ||
| CC | 15E | 5745.0 - 5825.0 | 0.00562 |
| Output power listed is average conducted. This device supports IEEE 802.11a (Wi-Fi 2) with a 20 MHz bandwidth mode and IEEE 802.11n (Wi-Fi 4) with a 20 MHz, 40 MHz bandwidth mode. For body worn and extremities operation this device has been tested touched to the phantom and meets FCC RF exposure guidelines. The highest reported SAR for body-worn and extremities SAR exposure conditions are 0.13 W/kg and 0.04 W/kg, respectively. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
| Mail To: |