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Integra EZ Oxygen Concentrator

FDA UDI

Class II (US FDA UDI)

by Caire Inc.

Identity

Trade Name
Integra EZ Oxygen Concentrator FDA UDI
Generic Name
Stationary oxygen concentrator FDA UDI
Device Name
Stationary Oxygen Concentrator 1-10 LPM, Non-OM, 220 Volt FDA UDI
Model / Reference
9623-SEQ FDA UDI
Description
Stationary Oxygen Concentrator 1-10 LPM, Non-OM, 220 Volt FDA UDI

Identifiers

Primary DI / UDI-DI
M7669623SEQ0 FDA UDI
510(k) Number
K042262 FDA UDI
FDA Product Code
CAW FDA UDI
GMDN Term
Stationary oxygen concentrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5440 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Stationary oxygen concentrator

Integra EZ Oxygen Concentrator by Caire Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stationary oxygen concentrator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Caire Inc.

Sources (1)

  • FDA UDI 28c7054a-2e06-41f9-9112-fb9d5110d6f5 34 fields · synced May 31, 2026