Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009694883

FEI Number

3009694883

Entity Name

REITER-HG GEIGER KUNSTSTOFFTECHNIK GMBH

City/State/Country

Hilpoltstein Bavaria, DE

Establishment Address

An der Autobahn L 5, Hilpoltstein Bavaria 91161, DE

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Reiter-HG Geiger Kunststofftechnik GmbH (Owner Number: 10087380)

Owner / Operator Contact Address

An der Autobahn L 5, Hilpoltstein, DE-BY 91161, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

DRAEGER SORB

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BSF	Absorber, Carbon-Dioxide	Anesthesiology	Class 1	868.5310	2023-02-20

Official Correspondent

Eva Soehnlein

US Agent Details

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

Related Public Records

Same Entity

Reiter-HG Geiger Kunststofftechnik GmbH

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0006-2008	Datex Ohmeda, Inc	1	GE Disposable Multi Absorber Canister used with EZchange Module for the Aisys, Avance, Aespire Anesthesia systems. The EZchange Module is an optional accessory for these anesthesia systems.

Similar Registrations

Registration Number	Establishment Name	Location
8010042	MAQUET CRITICAL CARE AB	SOLNA Stockholm, SE
3002807637	MOLECULAR PRODUCTS LTD	HARLOW Essex, GB
3016904853	SAINT JONES MANAGEMENT LP EOOD	Sofia Sofia-Grad, BG
1066427	INFINIUM MEDICAL, INC.	Largo, FL, US
3034669683	HUZHOU JUNDA INDUSTRY CO., LTD.	Anji Zhejiang, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009694883. Last updated year: 2026. Please use registration number 3009694883 when referencing this establishment in official correspondence.