MEDXPRESS.PRO

FDA Device Registration & Listing · Leuven Vlaams Brabant, BE · Registration 3017884667

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
3017884667
FEI Number
3017884667
Entity Name
MEDXPRESS.PRO
City/State/Country
Leuven Vlaams Brabant, BE
Establishment Address
Slachthuislaan 1, Bus 102, Leuven Vlaams Brabant 3000, BE
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
MedXPress.Pro (Owner Number: 10079948)
Owner / Operator Contact Address
Slachthuislaan 1, Bus 102, Leuven, BE-VBR 3000, BE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

EZDRAPE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PUI Drape, Surgical, Exempt General, Plastic Surgery Class 2 878.4370 2024-11-21

Official Correspondent

Stien Beyens

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

MedXPress.Pro
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 3017884667. Last updated year: 2026. Please use registration number 3017884667 when referencing this establishment in official correspondence.
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