microlife BP3GU1-8X

by Microlife USA, Inc.

microlife BP3GU1-8X is a Class II device made by Microlife USA, Inc., listed in FDA GUDID since 12 Jul 2024 (UDI-DI 00642632396009), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00642632396009 UDI-DI	Date12 Jul 2024Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00642632396009

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: microlife
Generic name: Automatic-inflation electronic sphygmomanometer, portable, arm/wrist
Model / reference: BP3GU1-8X

Primary DI / UDI-DI: 00642632396009
FDA product code: DXN
GMDN term: Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

Device class: Class II
Regulation number: 870.1130
GUDID distribution status: In Commercial Distribution

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Properties

Lot / batch number
Serial number

Other properties (13, all answered No)