Identity
- Trade Name
- Vive FDA UDI
- Generic Name
- Physiologic-monitoring defibrillation system FDA UDI
- Device Name
- Blood Pressure Monitor Black FDA UDI
- Model / Reference
- DMD1001BLK FDA UDI
- Description
- Blood Pressure Monitor Black FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00861470000323 FDA UDI
- FDA Product Code
- DXN FDA UDI
- GMDN Term
- Physiologic-monitoring defibrillation system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1130 FDA UDI
- Commercial Distribution
- Not 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
Yes
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
MR Conditional FDA UDI
Vive by Vive Health Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Vive Health Llc
Sources (1)
- FDA UDI 4ca9ceed-24ec-46f4-b727-0d1deaa5c704 34 fields · synced May 30, 2026