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Halyard DAAU12

by Medical Action Industries Inc.

Halyard DAAU12 is a Class II device made by Medical Action Industries Inc., listed in FDA GUDID since 28 Oct 2026 (UDI-DI 10809160542088), registry data as of 9 Nov 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10809160542088 UDI-DI Date28 Oct 2026ListedStatusListed 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  • Withdrawn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
General surgical procedure kit, medicated
Model / reference
DAAU12
Primary DI / UDI-DI
10809160542088
FDA product code
LRO
GMDN term
General surgical procedure kit, medicated
Device class
Class II
Regulation number
878.4370
GUDID distribution status
In Commercial Distribution

Other devices from Medical Action Industries Inc.

See all devices from Medical Action Industries Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Combination product
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (7, all answered No)