Identity
- Trade Name
- RENPHO Blood Pressure Monitor FDA UDI
- Generic Name
- Transcutaneous central venous pressure sensor FDA UDI
- Model / Reference
- RP-BPM001S FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04897106770045 FDA UDI
- FDA Product Code
- DXN FDA UDI
- GMDN Term
- Transcutaneous central venous pressure sensor FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1130 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Transcutaneous central venous pressure sensor
RENPHO Blood Pressure Monitor by Joicom Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Transcutaneous central venous pressure sensor.
- RENPHO BLOOD PRESSURE MONITOR — JOICOM CORPORATION · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Joicom Corporation
Sources (1)
- FDA UDI af1c2cf4-d8a1-494c-809b-81ec9805c91e 32 fields · synced Jun 1, 2026