Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007697975

FEI Number

3007697975

Entity Name

EUROMI S.A.

City/State/Country

Andrimont Liege, BE

Establishment Address

Rue des Nouvelles Technologies, 11, ZI des Plenesses, Andrimont Liege 4821, BE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Euromi S.A. (Owner Number: 10056094)

Owner / Operator Contact Address

Rue des Nouvelles Technologies, 11, ZI des Plenesses, Andrimont, BE-WLG 4821, BE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K101413

PMA Number

N/A

All Registered Proprietary Names

NLF SYSTEM Kit 2 (EUROMI) LIPOMATIC / EVAMATIC EVA SP6

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QKL	Lipoaspirate Washing System For Aesthetic Body Contouring	General, Plastic Surgery	Class 2	878.5040	2025-12-01
QPB	System, Suction, Lipoplasty For Removal	General, Plastic Surgery	Class 2	878.5040	2018-08-27
QPB	System, Suction, Lipoplasty For Removal	General, Plastic Surgery	Class 2	878.5040	2018-08-27

Official Correspondent

Alicia Robert-Laschette

US Agent Details

Dan Stoller Business: CENIT Consulting LLC Email: contact@cenitconsulting.com Phone: (281) 3806919

Related Public Records

Same Entity

Euromi S.A.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007697975. Last updated year: 2026. Please use registration number 3007697975 when referencing this establishment in official correspondence.