MediChoice BTD002

by Owens & Minor Distribution, Inc.

MediChoice BTD002 is a Class I device made by Owens & Minor Distribution, Inc., listed in FDA GUDID since 31 Aug 2020 (UDI-DI 10885632136764), 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	Number10885632136764 UDI-DI	Date31 Aug 2020Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10885632136764

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: MediChoice
Generic name: Blood collection tube holder, single-use
Model / reference: BTD002

Primary DI / UDI-DI: 10885632136764
FDA product code: KST
GMDN term: Blood collection tube holder, single-use

Device class: Class I
Regulation number: 864.9125
GUDID distribution status: In Commercial Distribution

Other devices from Owens & Minor Distribution, Inc.

See all devices from Owens & Minor Distribution, Inc. →

Properties

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

Other properties (9, all answered No)