E.A.M BENELUX B.V

FDA Device Registration & Listing · ALMERE Flevoland, NL · Registration 3042175944

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3042175944
FEI Number
3042175944
Entity Name
E.A.M BENELUX B.V
City/State/Country
ALMERE Flevoland, NL
Establishment Address
Korenbloemweg 79, ALMERE Flevoland 1338XT, NL
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
E.A.M Benelux B.V (Owner Number: 10094411)
Owner / Operator Contact Address
Korenbloemweg 79, ALMERE, NL-FL 1338XT, NL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

QF10

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JRL Unit, Filter, Membrane Clinical Chemistry Class 1 862.2050 2025-11-27

Official Correspondent

ILAN ABERMAN

US Agent Details

Ilan Aberman Business: Mentor Water Technologies USA, LLC Email: info.usa@mwt-nl.com Phone: (800) 2599107

Related Public Records

Same Entity

E.A.M Benelux B.V
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K812750 Instrumentation Laboratory CO IL 703, STAT SEPARATOR 1982-01-26

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042175944. Last updated year: 2026. Please use registration number 3042175944 when referencing this establishment in official correspondence.
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