← Back to catalogue

FlowMeter F1

FDA UDI

Class I (US FDA UDI)

by Imt Analytics Inc.

Identity

Trade Name
FlowMeter F1 FDA UDI
Generic Name
Anaesthesia/respiratory gas flowmeter tester FDA UDI
Device Name
Flowmeter, calibration, gas FDA UDI
Model / Reference
700.400.001 FDA UDI
Description
Flowmeter, calibration, gas FDA UDI

Identifiers

Primary DI / UDI-DI
07640214642837 FDA UDI
FDA Product Code
BXY FDA UDI
GMDN Term
Anaesthesia/respiratory gas flowmeter tester FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.2350 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Anaesthesia/respiratory gas flowmeter tester

FlowMeter F1 by Imt Analytics Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaesthesia/respiratory gas flowmeter tester.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Imt Analytics Inc.

Sources (1)

  • FDA UDI 317d1dc9-17d9-48b2-b67d-6243a527c029 33 fields · synced May 30, 2026