FOR LIFE GMBH

FDA Device Registration & Listing · BERLIN, DE · Registration 3003759552

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
3003759552
FEI Number
3003759552
Entity Name
FOR LIFE GMBH
City/State/Country
BERLIN, DE
Establishment Address
Am Studio 16, BERLIN 12489, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Unora GmbH (Owner Number: 9031211)
Owner / Operator Contact Address
Am Studio 16, --, BERLIN, DE-BE 12489, 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
EXG Bag, Urine Collecting, Ureterostomy Gastroenterology, Urology Class 1 876.5900 2002-04-15
EZQ Pouch, Colostomy Gastroenterology, Urology Class 1 876.5900 1997-08-04

Official Correspondent

Sascha Putzler

US Agent Details

Jerry Doane Business: Pragmatic Compliance dba FDAbasics Email: usagent@fdabasics.com Phone: (716) 7750533

Related Public Records

Same Entity

Unora 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 3003759552. Last updated year: 2026. Please use registration number 3003759552 when referencing this establishment in official correspondence.
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