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microlife BP3AQ1-1

by Microlife USA, Inc.

microlife BP3AQ1-1 is a Class II device made by Microlife USA, Inc., listed in FDA GUDID since 6 Jan 2017 (UDI-DI 00642632410095), 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

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00642632410095 UDI-DI Date6 Jan 2017ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
microlife
Generic name
Automatic-inflation electronic sphygmomanometer, non-portable
Model / reference
BP3AQ1-1
Primary DI / UDI-DI
00642632410095
FDA product code
DXN
GMDN term
Automatic-inflation electronic sphygmomanometer, non-portable
Device class
Class II
Regulation number
870.1130
GUDID distribution status
In Commercial Distribution

Related devices

Category: Automatic-inflation electronic sphygmomanometer, non-portable

Similar devices

Other devices filed under FDA product code DXN (System, Measurement, Blood-Pressure, Non-Invasive).

Other devices from Microlife USA, Inc.

See all devices from Microlife USA, Inc. →

Properties

  • Lot / batch number
Other properties (14, all answered No)