KIMETEC GMBH

FDA Device Registration & Listing · DITZINGEN Baden-Wurttemberg, DE · Registration 3000958046

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
3000958046
FEI Number
3000958046
Entity Name
KIMETEC GMBH
City/State/Country
DITZINGEN Baden-Wurttemberg, DE
Establishment Address
Dornierstr. 27, DITZINGEN Baden-Wurttemberg 71254, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Kimetec GmbH (Owner Number: 9026744)
Owner / Operator Contact Address
Dornierstr. 27, --, Ditzingen, DE-NOTA 71254, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

CBC TOURNIQUET

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HFS Shield, Nipple General Hospital Class 1 880.5630 2021-12-13
GAX Tourniquet, Nonpneumatic General, Plastic Surgery Class 1 878.5900 1996-07-02

Official Correspondent

No official correspondent registered.

US Agent Details

Alan Schwartz Business: mdi Consultants, Inc. Email: alan@mdiconsultants.com Phone: (516) 4829001

Related Public Records

Same Entity

Kimetec GmbH
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 3000958046. Last updated year: 2026. Please use registration number 3000958046 when referencing this establishment in official correspondence.
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