Medichoice YANK3001

by Owens & Minor Distribution, Inc.

Medichoice YANK3001 is a Class II device made by Owens & Minor Distribution, Inc., listed in FDA GUDID since 20 Aug 2016 (UDI-DI 10885632101144), 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	Number10885632101144 UDI-DI	Date20 Aug 2016Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10885632101144

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Medichoice
Generic name: Surgical/emergency suction cannula, non-illuminating, single-use
Model / reference: YANK3001

Primary DI / UDI-DI: 10885632101144
FDA product code: JOL
GMDN term: Surgical/emergency suction cannula, non-illuminating, single-use

Device class: Class II
Regulation number: 880.6740
GUDID distribution status: In Commercial Distribution

Similar devices in this category

Other devices filed under Surgical/emergency suction cannula, non-illuminating, single-use.

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Properties

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

Other properties (9, all answered No)