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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
Anaesthesia gas flowmeter FDA UDI
Device Name
Flow sensor SpiroQuant H FDA UDI
Model / Reference
SpiroQuant H FDA UDI
Description
Flow sensor SpiroQuant H FDA UDI

Identifiers

Catalog Number
07-00-0005 FDA UDI
Primary DI / UDI-DI
04036616005852 FDA UDI
FDA Product Code
BYR FDA UDI
GMDN Term
Anaesthesia gas flowmeter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.2875 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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 — 130 Millimeter FDA UDI
Length — 200 Millimeter FDA UDI
Width — 200 Millimeter FDA UDI

Category: Anaesthesia gas flowmeter

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

Similar devices

Also classified as Anaesthesia gas flowmeter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7d0ed05d-315b-4cee-9369-3fa0b241fcf4 37 fields · synced Jun 1, 2026