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3CP™ Centrifuge Kit 1

by Reapplix ApS 2 variants

3CP™ Centrifuge Kit 1 is a Class II device made by Reapplix ApS, listed in FDA GUDID since 3 Apr 2019 (UDI-DI 05714188308067), not in commercial distribution (GUDID) as of 22 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05714188308067 UDI-DI Date3 Apr 2019ListedStatusListed GUDID: not in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
3CP™ Centrifuge Kit
Generic name
Haematological concentrate system centrifuge
Model / reference
1
Primary DI / UDI-DI
05714188308067
FDA product code
PMQ
GMDN term
Haematological concentrate system centrifuge
Device class
Class II
Regulation number
864.9245
GUDID distribution status
Not in Commercial Distribution

Other devices from Reapplix ApS

See all devices from Reapplix ApS →

Properties

  • Prescription use
  • Convenience kit
  • Lot / batch number
Other properties (12, all answered No)