Halyard LIFP031_0005

by Avid Medical, Inc.

Halyard LIFP031_0005 is a Class I device made by Avid Medical, Inc., listed in FDA GUDID since 11 Dec 2020 (UDI-DI 10809160315262), 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number10809160315262 UDI-DI	Date11 Dec 2020Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10809160315262

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Halyard
Generic name: Laboratory specimen/material barcode label
Model / Ref / Catalog: LIFP031_0005, LIFP031

Primary DI / UDI-DI: 10809160315262
FDA product code: LYV
GMDN term: Laboratory specimen/material barcode label

Device class: Class I
Regulation number: 878.4800
GUDID distribution status: In Commercial Distribution

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Properties

Supplied sterile
Single use
Prescription use
Premarket exempt
Lot / batch number
Expiration date

Other properties (9, all answered No)