Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011213695

FEI Number

3011213695

Entity Name

AHLSTROM GERMANY GMBH

City/State/Country

Barenstein Saxony, DE

Establishment Address

Niederschlag 1, Barenstein Saxony 09471, DE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Ahlstrom Germany GmbH (Owner Number: 10092257)

Owner / Operator Contact Address

Niederschlag 1, Bärenstein, DE-SN 09471, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

AutoCollect card GenSaver card BioSample 2 Card LipidSaver Card 5 Circles card HemaSep card BioSample Card

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NNK	Container, Specimen Mailer And Storage, Non-Sterile	Pathology	Class 1	864.3250	2024-12-18

Official Correspondent

Jana Goss

US Agent Details

Ariel Gragnolati Business: Ahlstrom Filtration LLC Email: ariel.gragnolati@ahlstrom.com Phone: (860) 9976134

Related Public Records

Same Entity

Ahlstrom Germany 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 3011213695. Last updated year: 2026. Please use registration number 3011213695 when referencing this establishment in official correspondence.