LEMER-PAX

FDA Device Registration & Listing · Carquefou Loire-Atlantique, FR · Registration 3003808764

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
3003808764
FEI Number
3003808764
Entity Name
LEMER-PAX
City/State/Country
Carquefou Loire-Atlantique, FR
Establishment Address
Lieu-Dit La Haute Foret, 14 Avenue Syrma, Carquefou Loire-Atlantique 44470, FR
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
Lemer-Pax (Owner Number: 9050676)
Owner / Operator Contact Address
14 Avenue Syrma, Active-Malabry, Carquefou, FR-44 F-44240, FR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

EASYVIEW EASYSQUEEZE MEDICLIC

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KPY Shield, Protective, Personnel Radiology Class 1 892.6500 2002-04-11
IWR Holder, Syringe, Lead Radiology Class 1 892.6500 2002-04-11

Official Correspondent

No official correspondent registered.

US Agent Details

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

Related Public Records

Same Entity

Lemer-Pax
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 3003808764. Last updated year: 2026. Please use registration number 3003808764 when referencing this establishment in official correspondence.
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