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POM EZ-Lite MF

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
POM EZ-Lite MF FDA UDI
Generic Name
Capnography oxygen mask FDA UDI
Device Name
Adult Procedural Oxygen Mask - Medium Concentration and CO2 Monitoring (Male to Female) FDA UDI
Model / Reference
1003-MF FDA UDI
Description
Adult Procedural Oxygen Mask - Medium Concentration and CO2 Monitoring (Male to Female) FDA UDI

Identifiers

Catalog Number
1003-MF FDA UDI
Primary DI / UDI-DI
10851438008116 FDA UDI
FDA Product Code
CCK FDA UDI
GMDN Term
Capnography oxygen mask FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1400 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Capnography oxygen mask

POM EZ-Lite MF by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Capnography oxygen mask.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 61eb5097-861d-44d5-ac52-42ae287aa1d5 36 fields · synced Jun 7, 2026