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Starplex Specimen Container WB902-SO-OR

by Starplex Scientific, Inc.

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00840165500553 UDI-DI Date7 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  • Withdrawn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
Starplex Specimen Container
Generic Name
General specimen container IVD, no additive/medium
Model / Reference
WB902-SO-OR
Primary DI / UDI-DI
00840165500553
FDA Product Code
FMH
GMDN Term
General specimen container IVD, no additive/medium
Device Class
Class I
Regulation Number
864.3250
GUDID distribution status
In Commercial Distribution

Other devices from Starplex Scientific, Inc.

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Properties

  • Sterile
  • Single Use
  • Premarket Exempt

Other properties (11)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No