← Back to catalogue

Airgas Healthcare

FDA UDI

Class I (US FDA UDI)

by Airgas Usa Llc

Identity

Trade Name
Airgas Healthcare FDA UDI
Generic Name
Pulmonary function analysis system, adult FDA UDI
Device Name
Used for calibrating analyzers that are used in testing related to pulmonary functions, cardiac output, and metabolic studies. FDA UDI
Model / Reference
Device Gas FDA UDI
Description
Used for calibrating analyzers that are used in testing related to pulmonary functions, cardiac output, and metabolic studies. FDA UDI

Identifiers

Catalog Number
Pulmonary Function Gas FDA UDI
Primary DI / UDI-DI
00819601020030 FDA UDI
FDA Product Code
BXK FDA UDI
GMDN Term
Pulmonary function analysis system, adult FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6400 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Pulmonary function analysis system, adult

Airgas Healthcare by Airgas Usa Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulmonary function analysis system, adult.

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
Airgas Usa Llc

Sources (1)

  • FDA UDI 9b890d0a-91f8-4636-a35d-6a6669d52c28 36 fields · synced May 30, 2026