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Halyard SETA003-01_0013

by Avid Medical, 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 Number10809160351673 UDI-DIDate1 Jun 2021ListedStatusListed 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  • Withdrawn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
Halyard
Generic Name
Obstetrical/gynaecological surgical procedure kit, non-medicated, single-use
Model / Ref / Catalog
SETA003-01_0013, SETA003-01
Primary DI / UDI-DI
10809160351673
FDA Product Code
OKV
GMDN Term
Obstetrical/gynaecological surgical procedure kit, non-medicated, single-use
Device Class
Class II
Regulation Number
884.4520
GUDID distribution status
In Commercial Distribution

Related devices

Category: Obstetrical/gynaecological surgical procedure kit, non-medicated, single-use

Other devices from Avid Medical, Inc.

See all devices from Avid Medical, Inc. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Convenience Kit
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (7)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No