Identity
- Trade Name
- VASERlipo Accessories EUDAMEDVASER FDA UDI
- Generic Name
- Foot-switch, electrical FDA UDI
- Device Name
- VASER ADVANCED INSTRUMENTATION KIT EUDAMEDFDA UDI
- Model / Reference
- 115-0011 EUDAMEDFDA UDI
- Description
- VASER ADVANCED INSTRUMENTATION KIT FDA UDI
Identifiers
- Catalog Number
- 115-0011 FDA UDI
- Primary DI / UDI-DI
- 00816995027447 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00816995027447 EUDAMED
- FDA Product Code
- MUU FDA UDI
- EMDN Code
- L250399 LIPOSUCTION INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Foot-switch, electrical FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 878.5040 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
Category: Foot-switch, electrical
Vaser by Solta Medical, Inc. — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Foot-switch, electrical.
- ElectrodeCRF — Cambridge Interventional LLC · Class IIb
- ElectrodeCRF — Cambridge Interventional LLC · Class IIb
- Alligature-E — Alan Electronic Systems Private Limited · Class IIb
- Sonicure — Surgnova Healthcare Technologies (Zhejiang) Co., Ltd. · U
- Arthrex® — Arthrex, Inc. · Class I
- CableAME — Cambridge Interventional LLC · Class IIb
- CORE — Stryker Corp. · Class II
- PowerPack — MICROLINE SURGICAL, INC. · Class II
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDD | — | Class II | Unknown |
| 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
- Solta Medical, Inc.
Sources (2)
- FDA UDI 357bef7f-6ba6-479a-971b-e2d185e7fcf8 34 fields · synced Jun 19, 2026
- EUDAMED 372bda62-efcf-424c-b570-86eb5ea1c225 61 fields · synced Jun 19, 2026