Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010037894

FEI Number

3010037894

Entity Name

SCHMITZ medical GmbH

City/State/Country

Wickede North Rhine-Westphalia, DE

Establishment Address

Zum Ostenfeld 29, Wickede North Rhine-Westphalia 58739, DE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Schmitz medical GmbH (Owner Number: 10050373)

Owner / Operator Contact Address

Zum Ostenfeld 29, Wickede, DE-NW 58739, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

DIAMOND 40 LK DIAMOND 40 K DIAMOND 60 BLK DIAMOND 50 BK accessories

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FQO	Table, Operating-Room, Ac-Powered	General, Plastic Surgery	Class 1	878.4960	2015-11-10

Official Correspondent

Schmitz medical GmbH

US Agent Details

Yong Sun Business: Emergo Global Representation LLC Email: USAgent@ul.com Phone: (512) 3279997

Related Public Records

Same Entity

Schmitz medical 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-0036-2024	Getinge Usa Sales Inc	1	Meera Mobile Operating Table-to support and position the patient immediately before, during and after surgical interventions as well as for examination and treatment. Model Number: 7200.01F2

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010037894. Last updated year: 2026. Please use registration number 3010037894 when referencing this establishment in official correspondence.