CLERAD

FDA Device Registration & Listing · Clermont-Ferrand Puy-de-Dome, FR · Registration 3009518669

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
3009518669
FEI Number
3009518669
Entity Name
CLERAD
City/State/Country
Clermont-Ferrand Puy-de-Dome, FR
Establishment Address
184-186 avenue Gustave Flaubert, Clermont-Ferrand Puy-de-Dome 63000, FR
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
CLERAD (Owner Number: 10041828)
Owner / Operator Contact Address
15 rue Patrick Depailler, Clermont-Ferrand, FR-63 63000, FR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

KUBTEC GammaPRO GAMMA SUP II

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IZD Probe, Uptake, Nuclear Radiology Class 1 892.1320 2012-09-07

Official Correspondent

Philippe BRETTE

US Agent Details

RICK KILGUS Business: MINVASIVE SURGICAL Email: r.kilgus@minvasivesurgical.com Phone: (401) 2892223

Related Public Records

Same Entity

CLERAD
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 3009518669. Last updated year: 2026. Please use registration number 3009518669 when referencing this establishment in official correspondence.
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