CHP Handpiece

FDA UDI

Class I (US FDA UDI)

by Nouvag AG

Identity

Trade Name: CHP Handpiece FDA UDI
Generic Name: Liposuction system FDA UDI
Device Name: Conform Cannula Handpiece FDA UDI
Model / Reference: 5077NOU FDA UDI
Description: Conform Cannula Handpiece FDA UDI

Identifiers

Primary DI / UDI-DI: ENOU5077NOU0 FDA UDI
FDA Product Code: GEY FDA UDI
GMDN Term: Liposuction system FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4820 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Liposuction system

CHP Handpiece by Nouvag AG — Class I — 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

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 I	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Nouvag AG

Sources (1)

FDA UDI 7e31f0c0-0405-41a3-be57-b81a41841d81 34 fields · synced Jun 1, 2026