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Flow sensor

FDA UDI

Class I (US FDA UDI)

by Honeywell Healthcare Solutions GmbH

Identity

Trade Name
Flow sensor FDA UDI
Generic Name
Breathing circuit gas-flow sensor, reusable FDA UDI
Device Name
Flow sensor SpiroQuant A+ FDA UDI
Model / Reference
SpiroQuant A+ FDA UDI
Description
Flow sensor SpiroQuant A+ FDA UDI

Identifiers

Catalog Number
1000470 FDA UDI
Primary DI / UDI-DI
04036616001809 FDA UDI
FDA Product Code
BXP FDA UDI
GMDN Term
Breathing circuit gas-flow sensor, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.2885 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Height — 40 Millimeter FDA UDI
Length — 110 Millimeter FDA UDI
Width — 140 Millimeter FDA UDI

Category: Breathing circuit gas-flow sensor, reusable

Flow sensor by Honeywell Healthcare Solutions GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Breathing circuit gas-flow sensor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b997ae32-d4b2-4beb-a925-848dfe126040 36 fields · synced Jun 8, 2026