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Halyard 05710

by O&M Halyard Inc.

Listed FDA GUDID listing, not in commercial distribution

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 Number10680651057102 UDI-DI Date15 Sep 2016ListedStatusListed GUDID: not 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  • Withdrawn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
General surgical procedure kit, non-medicated, single-use
Model / Ref / Catalog
05710, 76092-ACM5710
Primary DI / UDI-DI
10680651057102
FDA Product Code
KKX
GMDN Term
General surgical procedure kit, non-medicated, single-use
Device Class
Class II
Regulation Number
878.4370
GUDID distribution status
Not in Commercial Distribution

Other devices from O&M Halyard Inc.

See all devices from O&M Halyard Inc. →

Properties

  • Sterile
  • Single Use
  • Lot / Batch Number

Other properties (11)

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