Identity
- Trade Name
- Injection cannula 3 FDA UDI
- Generic Name
- Liposuction system FDA UDI
- Model / Reference
- 10001184 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04260277174460 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
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Liposuction system
Injection cannula 3 by Möller Medical GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Liposuction system.
- ORIGINS — Solta Medical, Inc. · Class II
- Hydrophobic Filter-set — Human Med AG · Class II
- MicroAire® — MicroAire Surgical Instruments LLC · Class II
- AYON Base Tower — Apyx Medical Corporation · Class II
- 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:
- Liposat Pro — Möller Medical GmbH
- Liposat Pro plus — 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Möller Medical GmbH
Sources (1)
- FDA UDI 133392ce-2fd4-428b-9062-91965a3d95cf 34 fields · synced Jun 9, 2026