ADMEDES GMBH

FDA Device Registration & Listing · PFORZHEIM Baden-Wurttemberg, DE · Registration 3003956144

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
3003956144
FEI Number
3003956144
Entity Name
ADMEDES GMBH
City/State/Country
PFORZHEIM Baden-Wurttemberg, DE
Establishment Address
RASTATTER STRASSE 15, PFORZHEIM Baden-Wurttemberg 75179, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
ADMEDES GMBH (Owner Number: 9077299)
Owner / Operator Contact Address
RASTATTER STRASSE 15, PFORZHEIM, DE-BW 75179, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NIM Stent, Carotid Unknown Class 3 N/A 2008-01-03

Official Correspondent

Axel Pfrommer

US Agent Details

Craig Ball Email: cball@admedes.com Phone: (650) 2797952

Related Public Records

Same Entity

ADMEDES GMBH
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003956144. Last updated year: 2026. Please use registration number 3003956144 when referencing this establishment in official correspondence.
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