ANDRATEC GMBH

FDA Device Registration & Listing · Koblenz Rhineland-Palatinate, DE · Registration 3011668114

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
3011668114
FEI Number
3011668114
Entity Name
ANDRATEC GMBH
City/State/Country
Koblenz Rhineland-Palatinate, DE
Establishment Address
Kastorstr, 3, Koblenz Rhineland-Palatinate 56068, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
AndraTec GmbH (Owner Number: 10090560)
Owner / Operator Contact Address
Kastorstr, Koblenz, DE-RP 56068, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Andreas Kohl

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GAE Snare, Surgical General, Plastic Surgery Class 1 878.4800 2024-04-12

Official Correspondent

No official correspondent registered.

US Agent Details

Maik Endler Business: Sobel Consultancy Email: localrepresentation@sobelconsult.com Phone: (307) 3950846

Related Public Records

Same Entity

AndraTec 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 3011668114. Last updated year: 2026. Please use registration number 3011668114 when referencing this establishment in official correspondence.
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