ASSAMED GMBH

FDA Device Registration & Listing · BEXBACH Saarland, DE · Registration 3004483571

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
3004483571
FEI Number
3004483571
Entity Name
ASSAMED GMBH
City/State/Country
BEXBACH Saarland, DE
Establishment Address
MUNCHWIESER STR. 4, BEXBACH Saarland 66450, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ASSAMED GMBH (Owner Number: 9060071)
Owner / Operator Contact Address
MUNCHWIESER STR. 4, --, BEXBACH, DE-NOTA 66450, 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
GBX Catheter, Irrigation General, Plastic Surgery Class 1 878.4200 2004-02-25

Official Correspondent

No official correspondent registered.

US Agent Details

Franz Menean Business: MEDAGENT Inc. Email: mail@medagent-usa.com Phone: (603) 5702039

Related Public Records

Same Entity

ASSAMED 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 3004483571. Last updated year: 2026. Please use registration number 3004483571 when referencing this establishment in official correspondence.
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