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MediPure Laser Gas Mixture

FDA UDI

Class I (US FDA UDI)

by Linde Gas & Equipment Inc.

Identity

Trade Name
MediPure Laser Gas Mixture FDA UDI
Generic Name
Laser-generating gas FDA UDI
Device Name
Laser Gas Mixtures (of Specified Concentration) Gas, Laser Generating - Laser Gas FDA UDI
Model / Reference
1 FDA UDI
Description
Laser Gas Mixtures (of Specified Concentration) Gas, Laser Generating - Laser Gas FDA UDI

Identifiers

Primary DI / UDI-DI
00850046301186 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

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

Category: Laser-generating gas

MediPure Laser Gas Mixture by Linde Gas & Equipment Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laser-generating gas.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 505cbba0-4df1-4724-909a-25396db227ad 33 fields · synced Sep 18, 2026