PATIENT MONITOR CABLE PHILIPS (AGILENT) 12 pins
EUDAMEDFDA UDIClass I (EU MDR)
by Sophysa
Identity
- Trade Name
- PATIENT MONITOR CABLE PHILIPS (AGILENT) 12 pins EUDAMEDSOPHYSA FDA UDI
- Generic Name
- Electrical-only medical device connection cable, reusable FDA UDI
- Device Name
- PATIENT MONITOR CABLE EUDAMEDPatient Monitor Cable Philips (Agilent) 12 pins FDA UDI
- Model / Reference
- PSO-MC01 EUDAMEDFDA UDI
- Description
- Patient Monitor Cable Philips (Agilent) 12 pins FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03760124130690 EUDAMEDFDA UDI
- Basic UDI-DI
- 376012413PSOMCX000BS EUDAMED
- 510(k) Number
- K062584 FDA UDI
- FDA Product Code
- GWM FDA UDI
- EMDN Code
- Z12039099 VARIOUS INSTRUMENTS TO SUPPORT AND MONITOR VITAL SIGNS – OTHER EUDAMED
- GMDN Term
- Electrical-only medical device connection cable, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 882.1620 FDA UDI
- Market of Registration
- France EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
No
Implantable
No
Reusable
No
Contains Latex
No
Reprocessed
No
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
No
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
No
Serial Number
Yes
Expiration Date
No
Manufacturing Date
Yes
Discover the PATIENT MONITOR CABLE PHILIPS (AGILENT) 12 pins, a high-quality medical device designed for monitoring patients' vital signs. With its advanced features and robust design, this device is perfect for healthcare professionals who require precise and reliable measurements.
Authorization Coverage (2 countries)
Regulatory Authorizations
CE/MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 376012413PSOMCX000BS | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Sophysa
- EUDAMED SRN
- FR-MF-000002870
Sources (2)
- EUDAMED d0d630b5-9501-4b9c-b2fb-bb594d388570 61 fields · synced Oct 5, 2026
- FDA UDI fb6fc0b5-8b72-421c-b8dc-42228be8be8a 34 fields · synced May 30, 2026