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Halyard 88666

by O&M Halyard Inc.

Halyard 88666 is a Class II device made by O&M Halyard Inc., listed in FDA GUDID since 15 Mar 2017 (UDI-DI 10680651886665), 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 Number10680651886665 UDI-DI Date15 Mar 2017ListedStatusListed 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  • Withdrawn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
Instrument/equipment drape, single-use, sterile
Model / reference
88666
Primary DI / UDI-DI
10680651886665
FDA product code
KKX
GMDN term
Instrument/equipment drape, single-use, sterile
Device class
Class II
Regulation number
878.4370
GUDID distribution status
In Commercial Distribution

Related devices

Category: Instrument/equipment drape, single-use, sterile

Similar devices in this category

Other devices filed under Instrument/equipment drape, single-use, sterile.

Other devices from O&M Halyard Inc.

See all devices from O&M Halyard Inc. →

Properties

  • Supplied sterile
  • Single use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)