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NewLife Elite

FDA UDI

Class II (US FDA UDI)

by Caire Inc.

Identity

Trade Name
NewLife Elite FDA UDI
Generic Name
Stationary oxygen concentrator FDA UDI
Device Name
NEWLIFE ELITE OXYGEN CONCENTRATOR, 5LPM, 120V FDA UDI
Model / Reference
AS005-1 FDA UDI
Description
NEWLIFE ELITE OXYGEN CONCENTRATOR, 5LPM, 120V FDA UDI

Identifiers

Primary DI / UDI-DI
M766AS00510 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

NewLife Elite by Caire Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stationary oxygen concentrator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Caire Inc.

Sources (1)

  • FDA UDI 50df3070-d9ab-4af2-9620-eb91b553994d 33 fields · synced Jun 8, 2026