Airgas Healthcare

FDA UDI

Class I (US FDA UDI)

by Airgas Usa Llc

Identity

Trade Name: Airgas Healthcare FDA UDI
Generic Name: Laser-generating gas FDA UDI
Device Name: Gases utilized as a medium for various medical lasers. FDA UDI
Model / Reference: Device Gas FDA UDI
Description: Gases utilized as a medium for various medical lasers. FDA UDI

Identifiers

Catalog Number: Laser Gas FDA UDI
Primary DI / UDI-DI: 00819601020078 FDA UDI
FDA Product Code: NXF FDA UDI
GMDN Term: Laser-generating gas FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4810 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Laser-generating gas

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

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Laser Mixture — RED BALL OXYGEN COMPANY · Class I
Laser Gas Mixture — ROBERTS OXYGEN CO., INC. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Airgas Usa Llc

Sources (1)

FDA UDI d1175fb5-67c6-416a-91ee-4e811ee601c8 36 fields · synced May 31, 2026