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Masimo

FDA UDI

Class I (US FDA UDI)

by Airgas Usa Llc

Identity

Trade Name
Masimo FDA UDI
Generic Name
Ether anaesthesia vaporizer FDA UDI
Device Name
Description: 2% Desflurane, 5% CO2, 33% N2O, 55% O2, BAL. N2 ; Cylinder: UD; Valve: CGA 165; For calibration of medical analyzers in accordance with manufacturer's instructions. ; CE Marked FDA UDI
Model / Reference
ANESTHESIA CALIBRATION GAS FDA UDI
Description
Description: 2% Desflurane, 5% CO2, 33% N2O, 55% O2, BAL. N2 ; Cylinder: UD; Valve: CGA 165; For calibration of medical analyzers in accordance with manufacturer's instructions. ; CE Marked FDA UDI

Identifiers

Catalog Number
Z05NI5MUD0003 FDA UDI
Primary DI / UDI-DI
00819601022300 FDA UDI
FDA Product Code
BXK FDA UDI
GMDN Term
Ether anaesthesia vaporizer 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Pressure — 96 Pound per Square Inch FDA UDI
Total Volume — 145 Liter FDA UDI

Category: Ether anaesthesia vaporizer

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

Similar devices

Also classified as Ether anaesthesia vaporizer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Airgas Usa Llc

Sources (1)

  • FDA UDI de60a27d-6da4-44ae-9c2f-eb02f80d9327 37 fields · synced May 30, 2026