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Flow sensor SpiroQuant A+

by Honeywell Healthcare Solutions GmbH

Flow sensor SpiroQuant A+ (1000470) is a Class I device made by Honeywell Healthcare Solutions GmbH, listed in FDA GUDID since 22 Sep 2016 (UDI-DI 04036616001809), 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

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04036616001809 UDI-DI Date22 Sep 2016ListedStatusListed 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  • Withdrawn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
Flow sensor
Generic name
Breathing circuit gas-flow sensor, reusable
Model / Ref / Catalog
SpiroQuant A+, 1000470
Primary DI / UDI-DI
04036616001809
FDA product code
BXP
GMDN term
Breathing circuit gas-flow sensor, reusable
Device class
Class I
Regulation number
868.2885
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe
Size
Height — 40 Millimeter
Length — 110 Millimeter
Width — 140 Millimeter

Related devices

Category: Breathing circuit gas-flow sensor, reusable

Other devices from Honeywell Healthcare Solutions GmbH

See all devices from Honeywell Healthcare Solutions GmbH →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)