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3CP™ Counterbalance 2

by Reapplix ApS

3CP™ Counterbalance 2 is a Class I device made by Reapplix ApS, listed in FDA GUDID since 23 May 2019 (UDI-DI 05714188301808), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

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 Number05714188301808 UDI-DI Date23 May 2019ListedStatusListed GUDID: 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  • Withdrawn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™ Counterbalance
Generic name
Centrifuge tube counterbalance
Model / reference
2
Primary DI / UDI-DI
05714188301808
FDA product code
JQC
GMDN term
Centrifuge tube counterbalance
Device class
Class I
Regulation number
862.2050
GUDID distribution status
In Commercial Distribution

Related devices

Category: Centrifuge tube counterbalance

Other devices from Reapplix ApS

See all devices from Reapplix ApS →

Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)