Identity
- Trade Name
- V30 Console FDA UDI
- Generic Name
- Multi-modality skin surface treatment system generator FDA UDI
- Device Name
- V30 Console FDA UDI
- Model / Reference
- VTL40000 FDA UDI
- Description
- V30 Console FDA UDI
Identifiers
- Catalog Number
- VTL40000 FDA UDI
- Primary DI / UDI-DI
- 07290016746006 FDA UDI
- FDA Product Code
- PBX FDA UDIGEX FDA UDI
- GMDN Term
- Multi-modality skin surface treatment system generator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4400 FDA UDI878.4810 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
Yes
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Multi-modality skin surface treatment system generator
V30 Console by Viora Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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K162363 also covers:
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
- Viora Ltd
Sources (1)
- FDA UDI 54f6f461-45b3-4364-9245-436e137c14b2 36 fields · synced May 30, 2026