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DeVilbiss

FDA UDI

Class II (US FDA UDI)

by DeVilbiss Healthcare LLC.

Identity

Trade Name
DeVilbiss FDA UDI
Generic Name
Stationary oxygen concentrator FDA UDI
Device Name
5-liter oxygen concentrator FDA UDI
Model / Reference
525DS FDA UDI
Description
5-liter oxygen concentrator FDA UDI

Identifiers

Catalog Number
525DS FDA UDI
Primary DI / UDI-DI
00885304000846 FDA UDI
510(k) Number
K071397 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

No

FDA UDI

Category: Stationary oxygen concentrator

DeVilbiss by DeVilbiss Healthcare LLC. — 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

Sources (1)

  • FDA UDI 13a0b017-97c7-489e-aa6c-222fee15f5a2 37 fields · synced May 30, 2026