Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012228195

FEI Number

3012228195

Entity Name

TQ-SYSTEMS GMBH

City/State/Country

Seefeld Bavaria, DE

Establishment Address

Muehlstr. 2, Seefeld Bavaria 82229, DE

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

TQ-Systems GmbH (Owner Number: 10061461)

Owner / Operator Contact Address

Muehlstr. 2, Seefeld, DE-BY 82229, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

DAYSY Lady Comp

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LHD	Device, Fertility Diagnostic, Proceptive	Unknown	Class U	N/A	2019-10-21

Official Correspondent

Georg Unterlugauer

US Agent Details

Ralf Kuehn Business: President & CEO I TQ-Systems USA Inc. Email: Ralf.Kuehn@tq-group.com Phone: (817) 2627966

Related Public Records

Same Entity

TQ-Systems 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 3012228195. Last updated year: 2026. Please use registration number 3012228195 when referencing this establishment in official correspondence.