Identity
- Trade Name
- Revive RVT30 FDA UDI
- Generic Name
- Vibration platform exerciser, stationary FDA UDI
- Model / Reference
- JK 98 / RV 30-0 VBR E FDA UDI
Identifiers
- Primary DI / UDI-DI
- EJKP100003960B0 FDA UDI
- FDA Product Code
- BXB FDA UDI
- GMDN Term
- Vibration platform exerciser, stationary FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5380 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Vibration platform exerciser, stationary
Revive RVT30 by JK-Products GmbH — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- JK-Products GmbH
Sources (1)
- FDA UDI b5bdc6c5-49f8-495d-b874-6416a55b0868 32 fields · synced Jun 8, 2026