Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014326253

FEI Number

3014326253

Entity Name

REAPPLIX

City/State/Country

Birkerod Sjalland, DK

Establishment Address

Bregneroedvej 133A, st. th., Birkerod Sjalland 3460, DK

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Reapplix (Owner Number: 10057162)

Owner / Operator Contact Address

Bregneroedvej 133A, Birkerød, DK-85 3460, DK

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

3CP Counterbalance 3CP Centrifuge

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	2023-04-17

Official Correspondent

Henrik Brogaard Holmager

US Agent Details

MARGARET VERNON Business: Biologics Consulting Email: contracts@biologicsconsulting.com Phone: (720) 8833633

Related Public Records

Same Entity

Reapplix

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 3014326253. Last updated year: 2026. Please use registration number 3014326253 when referencing this establishment in official correspondence.