Identity
- Trade Name
- Vive FDA UDI
- Generic Name
- Portable sequential venous compression system FDA UDI
- Device Name
- Leg Compression Pump (Premium) FDA UDI
- Model / Reference
- RHB2025 FDA UDI
- Description
- Leg Compression Pump (Premium) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00810041983206 FDA UDI
- FDA Product Code
- IRP FDA UDI
- GMDN Term
- Portable sequential venous compression system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5650 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
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Portable sequential venous compression system
Vive by Vive Health Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Vive Health Llc
Sources (1)
- FDA UDI df255fb7-e4c1-49ed-8ddf-2e243303438a 33 fields · synced Jun 7, 2026