Identity
- Trade Name
- Liposat Pro plus FDA UDI
- Generic Name
- Liposuction system FDA UDI
- Device Name
- The "Liposat Pro plus" is a pump that is used in the field of aesthetic body contouring. The "Liposat Pro plus" is used to promote aqueous solutions for the production of tumescence local anesthesia as well as body-own, subcutaneous tissue and its components in the body. The pump "Liposat Pro plus" may only be used with the tube set "TLA Tubing Liposat Pro plus" and "Fat Tubing Liposat Pro plus" of the the Möller Medical GmbH. FDA UDI
- Model / Reference
- 00003974 FDA UDI
- Description
- The "Liposat Pro plus" is a pump that is used in the field of aesthetic body contouring. The "Liposat Pro plus" is used to promote aqueous solutions for the production of tumescence local anesthesia as well as body-own, subcutaneous tissue and its components in the body. The pump "Liposat Pro plus" may only be used with the tube set "TLA Tubing Liposat Pro plus" and "Fat Tubing Liposat Pro plus" of the the Möller Medical GmbH. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04260632792308 FDA UDI
- 510(k) Number
- K053451 FDA UDI
- FDA Product Code
- MUU FDA UDI
- GMDN Term
- Liposuction system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.5040 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
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: Liposuction system
Liposat Pro plus by Möller Medical GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Liposuction system.
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- MicroAire® — MicroAire Surgical Instruments LLC · Class II
- ORIGINS — Solta Medical, Inc. · Class II
- Alma LipoFlow System 50Hz — ALMA LASERS LTD. · Class II
- AirSculpt Handpiece — Millennium Medical Technologies, Inc. · Class II
Cleared under the same submission
K053451 also covers:
- Injection cannula 3 — Möller Medical GmbH
- Liposat Pro — Möller Medical GmbH
- Liposat power infiltration pump — Möller Medical GmbH
- Tubing for tumescent pump "Liposat" — Möller Medical GmbH
- Vacusat power — Möller Medical GmbH
- Vacusat power — Möller Medical GmbH
- Vibrasat Pro Console — Möller Medical GmbH
- Vibrasat Pro Wand — Möller Medical GmbH
- Vibrasat power — Möller Medical GmbH
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
- Möller Medical GmbH
Sources (1)
- FDA UDI 8b3fb72a-d1e0-43e1-8885-980ee9fdc4b7 34 fields · synced Jun 9, 2026