FCC ID VO9-H232
Blood measuring instrument
by Roche Diagnostics GmbH
Grantee Code: VO9 Product Code: H232
Latest application date: 2023-12-11
FCC ID Device Details
Operating Frequencies
| Frequency Range | Application Purpose | Final Action Date |
|---|---|---|
| 5180-5240 MHz | Original Equipment | 2023-12-11 |
| 2412-2462 MHz | Original Equipment | 2023-12-11 |
Exhibits
| Document | Type | Available | File |
|---|---|---|---|
| Users_Manual | Users Manual | 2023-12-11 | PDF 2.2 MB |
| Users_Manual_-_Regulatory_Information | Users Manual | 2023-12-11 | PDF 882.7 KB |
| Internal_Photos | Internal Photos | 2023-12-11 | PDF 606 KB |
| External_Photos | External Photos | 2023-12-11 | PDF 553.9 KB |
| ID_Label_Location_Info | ID Label/Location Info | 2023-12-11 | PDF 802.8 KB |
| Test_Setup_Photos | Test Setup Photos | 2023-12-11 | PDF 750.6 KB |
| Test_report_2G4WLAN_Host_radiated | Test Report | 2023-12-11 | PDF 2.8 MB |
| Test_report_2G4WLAN_conducted | Test Report | 2023-12-11 | PDF 5 MB |
| Test_report_5_GHz_WLAN | Test Report | 2023-12-11 | PDF 3.4 MB |
| Test_report_5_GHz_WLAN_-_Test_Results_Part_1 | Test Report | 2023-12-11 | PDF 5.5 MB |
| Test_report_5_GHz_WLAN_-_Test_Results_Part_2 | Test Report | 2023-12-11 | PDF 5.4 MB |
| Test_report_5_GHz_WLAN_-_Test_Results_Part_3 | Test Report | 2023-12-11 | PDF 5.3 MB |
| 2.911(d)(5)_Attestation_Letter | Attestation Statements | 2023-12-11 | PDF 113.1 KB |
| 2.911(d)(7)_Attestation_Letter | Attestation Statements | 2023-12-11 | PDF 281.1 KB |
| FCC_Confidentiality_Request | Cover Letter(s) | 2023-12-11 | PDF 998.6 KB |
| Original_Applicant_Authorization | Cover Letter(s) | 2023-12-11 | PDF 116.8 KB |
| Software_Security_Letter_UNII | Cover Letter(s) | 2023-12-11 | PDF 89.8 KB |
| U-NII_Device_Declaration_Letter | Cover Letter(s) | 2023-12-11 | PDF 1.7 MB |
| SAR_Caldata | RF Exposure Info | 2023-12-11 | PDF 2.9 MB |
| SAR_Test_Report | RF Exposure Info | 2023-12-11 | PDF 1.8 MB |
| SAR_Test_Setup_Photos | RF Exposure Info | 2023-12-11 | PDF 933.1 KB |
| Block_Diagram Metadata only | Block Diagram | PDF 571.1 KB | |
| Schematics Metadata only | Schematics | PDF 571.1 KB | |
| Schematics_Module Metadata only | Schematics | PDF 758.9 KB | |
| Antenna_information Metadata only | Operational Description | PDF 462.9 KB | |
| Operational_Description Metadata only | Operational Description | PDF 4.8 MB |
Application Information
| Application ID | JEJc+b65hdEzOKiC9EvGlA== |
|---|---|
| Final Action Date | 2023-12-11 |
| Application Purpose | Original Equipment |
| Applicant FRN | 0016954943 |
| Model | H232 |
| Frequency Range | 5180-5240 MHz |
| Equipment Class | NII - Unlicensed National Information Infrastructure TX |
| Device Description | Blood measuring instrument |
| Responsible Party | Christian Paulus, christian.paulus@roche.com  , +49621759 |
| Test Firm | Gerald Schmidt, cetecom advanced GmbH, gerald.schmidt@cetecomadvanced.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 conducted. This device supports IEEE 802.11a (Wi-Fi 2) with a 20 MHz bandwidth mode, IEEE 802.11n (Wi-Fi 4) with a 20 MHz, 40 MHz bandwidth mode and IEEE 802.11ac (Wi-Fi 5) with a 20 MHz, 40 MHz bandwidth mode. For body worn operation, this device has been tested and meets FCC RF exposure guidelines when used with an accessory that contains no metal and that positions the handset a minimum of 0 mm from the body. Use of other accessories may not ensure compliance with FCC RF exposure guidelines. End users must be informed of the body worn requirements for satisfying RF exposure compliance. The highest reported SAR for body-worn accessory and extremities are 0.47 W/kg, and 0.16 W/kg, respectively. |
Applications
| Application ID | Date | Purpose |
|---|---|---|
| JEJc+b65hdEzOKiC9EvGlA== | 2023-12-11 | Original Equipment |
| BmzKdu58Z69WCS4yrggHww== | 2023-12-11 | Original Equipment |
Equipment Authorization
Grants
TCB Grant - Application JEJc+b65hdEzOKiC9EvGlA==
| TCB | GRANT OF EQUIPMENT AUTHORIZATION |
TCB |
| Certification | ||
| Issued Under the Authority of the | ||
| Federal Communications Commission | ||
| By: |
|
cetecom advanced GmbH Untertuerkheimer Strasse 6-10 Saarbruecken, 66117 Germany |
Date of Grant: 12/11/2023 Application Dated: 12/11/2023 |
| 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-H232 |
| 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 |
| ND | 15E | 5180.0 - 5240.0 | 0.013 | ||
| ND | 15E | 5745.0 - 5825.0 | 0.005 |
| Output power listed is conducted. This device supports IEEE 802.11a (Wi-Fi 2) with a 20 MHz bandwidth mode, IEEE 802.11n (Wi-Fi 4) with a 20 MHz, 40 MHz bandwidth mode and IEEE 802.11ac (Wi-Fi 5) with a 20 MHz, 40 MHz bandwidth mode. For body worn operation, this device has been tested and meets FCC RF exposure guidelines when used with an accessory that contains no metal and that positions the handset a minimum of 0 mm from the body. Use of other accessories may not ensure compliance with FCC RF exposure guidelines. End users must be informed of the body worn requirements for satisfying RF exposure compliance. The highest reported SAR for body-worn accessory and extremities are 0.47 W/kg, and 0.16 W/kg, respectively. |
| 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 JEJc+b65hdEzOKiC9EvGlA==
| 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: 12/11/2023 Application Dated: 12/11/2023 |
| 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-H232 |
| 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 |
| ND | 15E | 5180.0 - 5240.0 | 0.013 | ||
| ND | 15E | 5745.0 - 5825.0 | 0.005 |
| Output power listed is conducted. This device supports IEEE 802.11a (Wi-Fi 2) with a 20 MHz bandwidth mode, IEEE 802.11n (Wi-Fi 4) with a 20 MHz, 40 MHz bandwidth mode and IEEE 802.11ac (Wi-Fi 5) with a 20 MHz, 40 MHz bandwidth mode. For body worn operation, this device has been tested and meets FCC RF exposure guidelines when used with an accessory that contains no metal and that positions the handset a minimum of 0 mm from the body. Use of other accessories may not ensure compliance with FCC RF exposure guidelines. End users must be informed of the body worn requirements for satisfying RF exposure compliance. The highest reported SAR for body-worn accessory and extremities are 0.47 W/kg, and 0.16 W/kg, respectively. |
| 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: |
|
cetecom advanced GmbH Untertuerkheimer Strasse 6-10 Saarbruecken, 66117 Germany |
Date of Grant: 12/11/2023 Application Dated: 12/11/2023 |
| 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-H232 |
| 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 | 0.011 |
| Output power listed is 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 4) with a 20 MHz, 40 MHz bandwidth mode. For body worn operation, this device has been tested and meets FCC RF exposure guidelines when used with an accessory that contains no metal and that positions the handset a minimum of 0 mm from the body. Use of other accessories may not ensure compliance with FCC RF exposure guidelines. End users must be informed of the body worn requirements for satisfying RF exposure compliance. The highest reported SAR for body-worn accessory and extremities are 0.47 W/kg, and 0.16 W/kg, respectively. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
EAS Grant - Application BmzKdu58Z69WCS4yrggHww==
| 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: 12/11/2023 Application Dated: 12/11/2023 |
| 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-H232 |
| 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 | 0.011 |
| Output power listed is 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 4) with a 20 MHz, 40 MHz bandwidth mode. For body worn operation, this device has been tested and meets FCC RF exposure guidelines when used with an accessory that contains no metal and that positions the handset a minimum of 0 mm from the body. Use of other accessories may not ensure compliance with FCC RF exposure guidelines. End users must be informed of the body worn requirements for satisfying RF exposure compliance. The highest reported SAR for body-worn accessory and extremities are 0.47 W/kg, and 0.16 W/kg, respectively. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
| Mail To: |