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LipoSurg

FDA UDI

Class II (US FDA UDI)

by Nouvag AG

Identity

Trade Name
LipoSurg FDA UDI
Generic Name
Liposuction system FDA UDI
Device Name
Surgical motor and infiltration system FDA UDI
Model / Reference
3362 FDA UDI
Description
Surgical motor and infiltration system FDA UDI

Identifiers

Primary DI / UDI-DI
ENOU33620 FDA UDI
FDA Product Code
FRN FDA UDI
GEY FDA UDI
GMDN Term
Liposuction system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5725 FDA UDI
878.4820 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

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Liposuction system

LipoSurg by Nouvag AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Liposuction system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nouvag AG

Sources (1)

  • FDA UDI ddb49f18-4f22-4cda-82be-fd33a986fbab 34 fields · synced May 30, 2026