Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005332796

FEI Number

3005332796

Entity Name

Eppendorf Manufacturing Corporation

City/State/Country

Enfield, CT, US

Establishment Address

175 Freshwater Blvd, Enfield, CT 06082, US

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

No US Agent registered (Local establishment).

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
3015286853	Eppendorf Polymere GmbH	Oldenburg Schleswig-Holstein, DE
8010471	EPPENDORF SE	HAMBURG, DE
3011544811	Eppendorf Zentrifugen GmbH	Leipzig Saxony, DE

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005332796. Last updated year: 2026. Please use registration number 3005332796 when referencing this establishment in official correspondence.