Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011544811

FEI Number

3011544811

Entity Name

Eppendorf Zentrifugen GmbH

City/State/Country

Leipzig Saxony, DE

Establishment Address

Portitzer Allee 15, Leipzig Saxony 04329, DE

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Eppendorf SE (Owner Number: 8010471)

Owner / Operator Contact Address

175 Freshwater Blvd., Enfield, CT 06082, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Centrifuge 5702; Centrifuge 5702 R; Centrifuge 5702 RH

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	2013-03-25

Official Correspondent

Denise Case

US Agent Details

Denise Case Business: Eppendorf North America Email: case.d@eppendorf.com Phone: (800) 6443405

Related Public Records

Same Entity

Eppendorf SE

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3005332796	Eppendorf Manufacturing Corporation	Enfield, CT, US
3015286853	Eppendorf Polymere GmbH	Oldenburg Schleswig-Holstein, DE
8010471	EPPENDORF SE	HAMBURG, DE

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011544811. Last updated year: 2026. Please use registration number 3011544811 when referencing this establishment in official correspondence.