Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014213278

FEI Number

3014213278

Entity Name

GEMU WERK GREMMEL & MULDERS GMBH

City/State/Country

Lehrte Lower Saxony, DE

Establishment Address

Hannoversche Str. 38, Lehrte Lower Saxony 31275, DE

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Gemu Werk Gremmel & Mulders GmbH (Owner Number: 10056572)

Owner / Operator Contact Address

Hannoversche Str. 38, Lehrte, DE-NI 31275, DE

Initial Importer Flag

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
MHW	Dressing, Compression	General Hospital	Class 1	880.5075	2017-12-22

Official Correspondent

Dietmar Gremmel

US Agent Details

Sam Shaffer Business: L&R USA INC. Email: sam.shaffer@us.LRmed.com Phone: (414) 8924157

Related Public Records

Same Entity

Gemu Werk Gremmel & Mulders 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 3014213278. Last updated year: 2026. Please use registration number 3014213278 when referencing this establishment in official correspondence.