Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017365972

FEI Number

3017365972

Entity Name

WEINMANN EMERGENCY MEDICAL TECHNOLOGY GMBH

City/State/Country

Hamburg, DE

Establishment Address

Frohboesestrasse 12, Hamburg 22525, DE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

WEINMANN Emergency Medical Technology GmbH (Owner Number: 10059708)

Owner / Operator Contact Address

Frohboesestrasse 12, Hamburg, DE-HH 22525, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K193191

PMA Number

N/A

All Registered Proprietary Names

MEDUMAT Easy CPR

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BTL	Ventilator, Emergency, Powered (Resuscitator)	Anesthesiology	Class 2	868.5925	2020-12-01

Official Correspondent

Florian Dietz

US Agent Details

Enrico Nikolai Business: WEINMANN Emergency LP Email: E.Nikolai@weinmann-emergency.com Phone: (770) 2742417

Related Public Records

Same Entity

WEINMANN Emergency Medical Technology GmbH

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K862192	U.O. Equipment Co.	RESUSCITATOR MODELS 10400/10500/10600/10700/10800	1986-07-07

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0004-2025	Mercury Enterprises, Inc. dba Mercury Medical	2	Neo-Tee T-Piece Resuscitator. Part Numbers 1050805, 1050832. For pediatric emergency respiratory support.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017365972. Last updated year: 2026. Please use registration number 3017365972 when referencing this establishment in official correspondence.