Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030303856

FEI Number

3030303856

Entity Name

GERMITEC

City/State/Country

Bordeaux Nouvelle-Aquitaine, FR

Establishment Address

19 rue Vauban, Bordeaux Nouvelle-Aquitaine 33000, FR

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

GERMITEC (Owner Number: 10091485)

Owner / Operator Contact Address

19 rue Vauban, Bordeaux, FR-NAQ 33000, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

DEN230067

PMA Number

N/A

All Registered Proprietary Names

CHRONOS

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
SCS	Ultraviolet Radiation Disinfection Chamber Device	General Hospital	Class 2	880.6511	2024-10-08

Official Correspondent

Jose DA GLORIA

US Agent Details

Keith KOBY Business: Germitec Email: k.koby@germitec.com Phone: (414) 8700306

Related Public Records

Same Entity

GERMITEC

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 3030303856. Last updated year: 2026. Please use registration number 3030303856 when referencing this establishment in official correspondence.