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Responsive Respiratory, Inc.

FDA UDI

Class I (US FDA UDI)

by Responsive Respiratory Inc.

Identity

Trade Name
Responsive Respiratory, Inc. FDA UDI
Generic Name
Anaesthesia/respiratory gas flowmeter tester FDA UDI
Device Name
Liter Meter, 0-2.5 LPM FDA UDI
Model / Reference
180-5004 FDA UDI
Description
Liter Meter, 0-2.5 LPM FDA UDI

Identifiers

Primary DI / UDI-DI
00851440007599 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

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Anaesthesia/respiratory gas flowmeter tester

Responsive Respiratory, Inc. by Responsive Respiratory 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

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Manufacturer

Sources (1)

  • FDA UDI fa2c2ac2-3aee-4794-acf7-1ede13ec9f6e 33 fields · synced May 30, 2026