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TrueBond TRIFlex Centrifuge, Drucker 00-389-009-002

by Drucker Diagnostics

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810052864815 UDI-DI Date8 Oct 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
TrueBond TRIFlex Centrifuge, Drucker
Generic Name
General-purpose centrifuge IVD
Model / Ref / Catalog
00-389-009-002
Primary DI / UDI-DI
00810052864815
FDA Product Code
JQC
GMDN Term
General-purpose centrifuge IVD
Device Class
Class I
Regulation Number
862.2050
GUDID distribution status
In Commercial Distribution

Other devices from Drucker Diagnostics

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Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Expiration Date: No
  • Manufacturing Date: No