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Mark 5 Nuvo 10

FDA UDI

Class II (US FDA UDI)

by Nidek Medical Products Inc.

Identity

Trade Name
MARK 5 NUVO 10 FDA UDI
Generic Name
Stationary oxygen concentrator FDA UDI
Device Name
230V OCSI 10LPM OXYGEN CONCENTRATOR -- PRIVATE LABELED FOR GCE MEDILINE, UK PLUG FDA UDI
Model / Reference
1005GCUK FDA UDI
Description
230V OCSI 10LPM OXYGEN CONCENTRATOR -- PRIVATE LABELED FOR GCE MEDILINE, UK PLUG FDA UDI

Identifiers

Catalog Number
1005GCUK FDA UDI
Primary DI / UDI-DI
00038214001575 FDA UDI
510(k) Number
K123738 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Stationary oxygen concentrator

Mark 5 Nuvo 10 by Nidek Medical Products 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

Sources (1)

  • FDA UDI ab35944c-ffc4-42dc-ab92-d6dc595c0fce 37 fields · synced May 30, 2026