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Specimen Collection Swab FASPS10

by Hlb Co., Ltd 12 variants

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 Number08809262394368 UDI-DI Date28 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  • Withdrawn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
Specimen Collection Swab
Generic Name
Oral/upper respiratory tract specimen collection swab
Model / Reference
FASPS10
Primary DI / UDI-DI
08809262394368
FDA Product Code
KXG
GMDN Term
Oral/upper respiratory tract specimen collection swab
Device Class
Class I
Regulation Number
880.6025
GUDID distribution status
In Commercial Distribution

Other devices from Hlb Co., Ltd

See all devices from Hlb Co., Ltd →

Properties

  • Sterile
  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

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