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Halyard MARS002-06_0002

by Avid Medical, Inc.

Halyard MARS002-06_0002 is a Class II device made by Avid Medical, Inc., listed in FDA GUDID since 29 Oct 2026 (UDI-DI 10809160542224), 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 Number10809160542224 UDI-DI Date29 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  • Withdrawn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
Urological surgical procedure kit, medicated, single-use
Model / Ref / Catalog
MARS002-06_0002, MARS002-06
Primary DI / UDI-DI
10809160542224
FDA product code
LRO
GMDN term
Urological surgical procedure kit, medicated, single-use
Device class
Class II
Regulation number
878.4370
GUDID distribution status
In Commercial Distribution

Other devices from Avid Medical, Inc.

See all devices from Avid Medical, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (8, all answered No)