EURORAD DEUX SIX

FDA Device Registration & Listing · ECKBOLSHEIM Bas-Rhin, FR · Registration 3003508021

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
3003508021
FEI Number
3003508021
Entity Name
EURORAD DEUX SIX
City/State/Country
ECKBOLSHEIM Bas-Rhin, FR
Establishment Address
2 RUE E. BUGATTI, ECKBOLSHEIM Bas-Rhin 67201, FR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
EURORAD DEUX SIX (Owner Number: 9032627)
Owner / Operator Contact Address
2 RUE E. BUGATTI, --, ECKBLOSHEIM, FR-NOTA 67201, FR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

EUROPROBE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IZD Probe, Uptake, Nuclear Radiology Class 1 892.1320 2003-04-18

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

EURORAD DEUX SIX
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
K942580 Neoprobe Corp. NEOPROBE 1000 PORTABLE RADIOISOTOPE DETECTOR AND ACCESSORIES 1995-02-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003508021. Last updated year: 2026. Please use registration number 3003508021 when referencing this establishment in official correspondence.
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