Halyard CNPD034_0012

by Avid Medical, Inc.

Halyard CNPD034_0012 is a Class II device made by Avid Medical, Inc., listed in FDA GUDID since 20 Aug 2021 (UDI-DI 10809160357613), 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	Number10809160357613 UDI-DI	Date20 Aug 2021Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10809160357613

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Halyard
Generic name: Peripheral anaesthesia single-administration set, non-medicated
Model / Ref / Catalog: CNPD034_0012, CNPD034

Primary DI / UDI-DI: 10809160357613
FDA product code: OGD
GMDN term: Peripheral anaesthesia single-administration set, non-medicated

Device class: Class II
Regulation number: 868.5120
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
Combination product
Premarket exempt
Lot / batch number
Expiration date

Other properties (7, all answered No)