Halyard VHWV009-13_0001

by Avid Medical, Inc.

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

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

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number10809160415658 UDI-DI	Date6 Jan 2024Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Halyard
Generic Name: General surgical procedure kit, medicated
Model / Ref / Catalog: VHWV009-13_0001, VHWV009-13

Primary DI / UDI-DI: 10809160415658
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 Avid Medical, Inc.

See all devices from Avid Medical, Inc. →

Properties

Sterile
Single Use
Prescription Use
Convenience Kit
Combination Product
Premarket Exempt
Lot / Batch Number
Expiration Date

Other properties (6)

Implantable: No
Contains Latex: No
Over-the-Counter: No
HCT/P: No
Serial Number: No
Manufacturing Date: No