Identity
- Trade Name
- Lipo-One® FDA UDI
- Generic Name
- Liposuction system cannula, single-use FDA UDI
- Device Name
- Disposable liposuction cannula FDA UDI
- Model / Reference
- 3mm x 28 cm - 24-hole FDA UDI
- Description
- Disposable liposuction cannula FDA UDI
Identifiers
- Catalog Number
- LC328024H FDA UDI
- Primary DI / UDI-DI
- 03760037734336 FDA UDI
- FDA Product Code
- MUU FDA UDI
- GMDN Term
- Liposuction system cannula, single-use 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
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Liposuction system cannula, single-use
Lipo-One® by Aesthetic Group — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Liposuction system cannula, single-use.
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- SUMMIT MEDICAL — Summit Medical, LLC · Class I
- Multi Rapid Extraction Cannula — Möller Medical GmbH · Class I
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
- Aesthetic Group
Sources (1)
- FDA UDI 650c1f1e-72bb-466d-90b8-637f95058f61 34 fields · synced May 30, 2026