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3C Patch® Device 1

by Reapplix ApS

3C Patch® Device 1 is a Class II device made by Reapplix ApS, listed in FDA GUDID since 19 Jul 2018 (UDI-DI 05714188502151), 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 Number05714188502151 UDI-DI Date19 Jul 2018ListedStatusListed 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  • Withdrawn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
3C Patch® Device
Generic name
Haematological concentrate system preparation kit, platelet concentration
Model / reference
1
Primary DI / UDI-DI
05714188502151
FDA product code
PMQ
GMDN term
Haematological concentrate system preparation kit, platelet concentration
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

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)