Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010394461

FEI Number

3010394461

Entity Name

HERMLE LABORTECHNIK GMBH

City/State/Country

Wehingen Baden-Wurttemberg, DE

Establishment Address

Siemensstr. 25, Wehingen Baden-Wurttemberg 78564, DE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

HERMLE LaborTechnik GmbH (Owner Number: 10093085)

Owner / Operator Contact Address

Siemensstr. 25, Wehingen, DE-BW 78564, 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
JQC	Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use	Clinical Chemistry	Class 1	862.2050	2025-03-28

Official Correspondent

Marco Sachsse

US Agent Details

Franz Menean Business: MEDAGENT Inc. Email: service@medagent.de Phone: (603) 5702039

Related Public Records

Same Entity

HERMLE LaborTechnik 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 3010394461. Last updated year: 2026. Please use registration number 3010394461 when referencing this establishment in official correspondence.