Identity
- Trade Name
- VASER FDA UDI
- Generic Name
- Ultrasonic surgical system generator FDA UDI
- Device Name
- 4.6 mm Skin Port Plug FDA UDI
- Model / Reference
- 130-0112 FDA UDI
- Description
- 4.6 mm Skin Port Plug FDA UDI
Identifiers
- Catalog Number
- 130-0112 FDA UDI
- Primary DI / UDI-DI
- 00850608002834 FDA UDI
- FDA Product Code
- MUU FDA UDI
- GMDN Term
- Ultrasonic surgical system generator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.5040 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
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Vaser by Solta Medical, Inc. — 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 |
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Manufacturer
- Manufacturer
- Solta Medical, Inc.
Sources (1)
- FDA UDI f2ec5cc4-ab95-4eee-97aa-5b22a140fe98 35 fields · synced Jun 1, 2026