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Halyard 39241

by O&M Halyard Inc.

Halyard 39241 is a Class II device made by O&M Halyard Inc., listed in FDA GUDID since 10 Sep 2016 (UDI-DI 10680651392418), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10680651392418 UDI-DI Date10 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

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  • Withdrawn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
Patient surgical drape, single-use
Model / Ref / Catalog
39241
Primary DI / UDI-DI
10680651392418
FDA product code
KKX
GMDN term
Patient surgical drape, single-use
Device class
Class II
Regulation number
878.4370
GUDID distribution status
In Commercial Distribution

Related devices

Category: Patient surgical drape, single-use

Other devices from O&M Halyard Inc.

See all devices from O&M Halyard Inc. →

Properties

  • Supplied sterile
  • Single use
  • Lot / batch number
Other properties (12, all answered No)