FCC ID PQC-OBRWRPBV1
Patient Monitoring
by Philips Medical Systems North America Co.
Grantee Code: PQC Product Code: OBRWRPBV1
Latest application date: 2016-08-17
FCC ID Device Details
| FCC ID | PQC-OBRWRPBV1 |
|---|---|
| Mirrors | fcc.id | gov | fccid.ai |
| Grantee Code | PQC |
| Product Code | OBRWRPBV1 |
| Applicant Business | Philips Medical Systems North America Co. 🇺🇸 |
| Related Domains |  philips.com |
| Equipment Class | Patient Monitoring |
| Test Firm | CTC advanced GmbH |
Operating Frequencies
| Frequency Range | Application Purpose | Final Action Date |
|---|---|---|
| 608-614 MHz | Original Equipment | 2016-08-17 |
Exhibits
| Document | Type | Available | File |
|---|---|---|---|
| User Manual Part 1 | Users Manual | 2017-02-13 | PDF 4.3 MB |
| User Manual Part 2 | Users Manual | 2017-02-13 | PDF 4.3 MB |
| Internal Photos | Internal Photos | 2017-02-13 | PDF 1 MB |
| External Photos | External Photos | 2017-02-13 | PDF 586.6 KB |
| Label | ID Label/Location Info | 2016-08-17 | PDF 427.5 KB |
| SAR_photos | Test Setup Photos | 2017-02-13 | PDF 870.6 KB |
| Test Setup Photos | Test Setup Photos | 2017-02-13 | PDF 1.1 MB |
| Test Report WMTS | Test Report | 2016-08-17 | PDF 1.4 MB |
| fcc_confidentiality request letter (permanent)_avalon cl wide range pod_finale v | Cover Letter(s) | 2016-08-17 | PDF 675.7 KB |
| fcc_confidentiality request letter (short-term) | Cover Letter(s) | 2016-08-17 | PDF 686.3 KB |
| SAR Report | RF Exposure Info | 2016-08-17 | PDF 1.2 MB |
| SAR_caldata | RF Exposure Info | 2016-08-17 | PDF 1.8 MB |
| Block Diagram Metadata only | Block Diagram | PDF 180.6 KB | |
| pcb Metadata only | Schematics | PDF 832.3 KB | |
| schematics Metadata only | Schematics | PDF 104.3 KB | |
| Operational Description Metadata only | Operational Description | PDF 696.5 KB | |
| Tune Up Info Metadata only | Parts List/Tune Up Info | PDF 687.2 KB |
Application Information
| Application ID | kLC8CR/TDZbzKf09IIN3/Q== |
|---|---|
| Final Action Date | 2016-08-17 |
| Application Purpose | Original Equipment |
| Applicant FRN | 0017950635 |
| Model | OBRWRPBV1 |
| Frequency Range | 608-614 MHz |
| Equipment Class | TNT - Licensed Non-Broadcast Transmitter Worn on Body |
| Device Description | Patient Monitoring |
| Responsible Party | Delroy Smith, Principal Scientist / Project Leader, delroy.smith@philips.com , + 1 978 659 3382 |
| Test Firm | Gerald Schmidt, CTC advanced GmbH, mail@ctcadvanced.com  , 49-681-598-0 |
| TCB Email | TCB@cetecom.com  |
| TCB Scope | B1: Commercial mobile radio services equipment in the following 47 CFR Parts 20, 22 (cellular), 24,25 (below 3 GHz) & 27 |
| Short-Term Confidentiality | Yes |
| Short-Term Confidentiality Date | 02/13/2017 |
| Long-Term Confidentiality | Yes |
| Grant Deferral | No |
| Modular Equipment | Does not apply |
| Composite Device | No |
| 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 | Power output listed is ERP. This device has been evaluated in specific co-located situations as indicated in this filing. The highest reported SAR for body-worn and simultaneous transmission use conditions are 0.66 W/kg and 0.70 W/kg, respectively. End-users must be provided with specific operating instructions for satisfying RF exposure compliance. |
Applications
| Application ID | Date | Purpose |
|---|---|---|
| kLC8CR/TDZbzKf09IIN3/Q== | 2016-08-17 | Original Equipment |
Equipment Authorization
Grants
TCB Grant - Application kLC8CR/TDZbzKf09IIN3/Q==
| 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: 08/17/2016 Application Dated: 08/17/2016 |
| Philips Medical Systems North America Co. |
| 3000 Minuteman Road |
| Andover, MA 01810-1099 |
| Attention: Delroy Smith , Principal Scientist / Project Leader |
| 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: | PQC-OBRWRPBV1 |
| Name of Grantee: | Philips Medical Systems North America Co. |
| Equipment Class: | Licensed Non-Broadcast Transmitter Worn on Body |
| Notes: | Patient Monitoring |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| 95H | 608.0 - 614.0 | 0.00001 | 1.0 PM | 29K2F7D |
| Power output listed is ERP. This device has been evaluated in specific co-located situations as indicated in this filing. The highest reported SAR for body-worn and simultaneous transmission use conditions are 0.66 W/kg and 0.70 W/kg, respectively. End-users must be provided with specific operating instructions for satisfying RF exposure compliance. |
EAS Grant - Application kLC8CR/TDZbzKf09IIN3/Q==
| COPY |
FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION |
COPY |
| Certification |
|
Philips Medical Systems North America Co. 3000 Minuteman Road Andover, MA 01810-1099 United States |
Date of Grant: 08/17/2016 Application Dated: 08/17/2016 |
| Attention: Delroy Smith , Principal Scientist / Project Leader |
| 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: | PQC-OBRWRPBV1 |
| Name of Grantee: | Philips Medical Systems North America Co. |
| Equipment Class: | Licensed Non-Broadcast Transmitter Worn on Body |
| Notes: | Patient Monitoring |
| Modular Type: | Does not apply |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| 95H | 608.0 - 614.0 | 0.00001 | 1.0 PM | 29K2F7D |
| Power output listed is ERP. This device has been evaluated in specific co-located situations as indicated in this filing. The highest reported SAR for body-worn and simultaneous transmission use conditions are 0.66 W/kg and 0.70 W/kg, respectively. End-users must be provided with specific operating instructions for satisfying RF exposure compliance. |
| Mail To: |