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Disposable Liposuction Cannula

FDA UDI

Class II (US FDA UDI)

by Aesthetic Group

Identity

Trade Name
DISPOSABLE LIPOSUCTION CANNULA FDA UDI
Generic Name
Liposuction system cannula, single-use FDA UDI
Device Name
4 mm x 28 cm - 3-hole Mercedes FDA UDI
Model / Reference
3-hole Mercedes FDA UDI
Description
4 mm x 28 cm - 3-hole Mercedes FDA UDI

Identifiers

Catalog Number
LC42803M FDA UDI
Primary DI / UDI-DI
03701068800157 FDA UDI
510(k) Number
K132353 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

Disposable Liposuction Cannula by Aesthetic Group — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Liposuction system cannula, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesthetic Group

Sources (1)

  • FDA UDI 21225b7e-586e-49f9-830d-96b15b9c1c79 36 fields · synced May 30, 2026