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VisionAire 3

FDA UDI

Class II (US FDA UDI)

by Airsep Corp.

Identity

Trade Name
VisionAire 3 FDA UDI
Generic Name
Stationary oxygen concentrator FDA UDI
Device Name
Oxygen Concentrator, 1-3 LPM, base model FDA UDI
Model / Reference
AS096-6 FDA UDI
Description
Oxygen Concentrator, 1-3 LPM, base model FDA UDI

Identifiers

Primary DI / UDI-DI
M638AS09660 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

VisionAire 3 by Airsep Corp. — 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
Airsep Corp.

Sources (1)

  • FDA UDI 562a26b3-0f33-498d-bd1b-2b4bf87d55e0 33 fields · synced Jun 8, 2026