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Transcend Axis 10-000202-00-00

by Transcend Biologics, LLC

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 Number00850045520465 UDI-DI Date6 Aug 2026ListedStatusListed 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  • Withdrawn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
Transcend Axis
Generic Name
Haematological concentrate system centrifuge
Model / Ref / Catalog
10-000202-00-00, 000202
Primary DI / UDI-DI
00850045520465
GMDN Term
Haematological concentrate system centrifuge
GUDID distribution status
In Commercial Distribution

Other devices from Transcend Biologics, LLC

See all devices from Transcend Biologics, LLC →

Properties

  • Convenience Kit
  • Serial Number

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No