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NATROX® Oxygen Wound Therapy

FDA UDI

Class II (US FDA UDI)

by Inotec Amd , Ltd.

Identity

Trade Name
NATROX® Oxygen Wound Therapy FDA UDI
Generic Name
Wound therapy oxygenator, single-use FDA UDI
Device Name
The NATROX® System provides oxygen to diffuse evenly over the wound bed under an occlusive dressing, constantly refreshing the oxygen supply to enhance the normal process of wound healing for chronic and hard-to-heal wounds with compromised oxygen delivery to healing tissue. A small diameter tube transmits the oxygen to the wound bed, where the wound is exposed to the oxygen atmosphere inside the Oxygen Delivery System (ODS), FDA UDI
Model / Reference
Oxygen Delivery System FDA UDI
Description
The NATROX® System provides oxygen to diffuse evenly over the wound bed under an occlusive dressing, constantly refreshing the oxygen supply to enhance the normal process of wound healing for chronic and hard-to-heal wounds with compromised oxygen delivery to healing tissue. A small diameter tube transmits the oxygen to the wound bed, where the wound is exposed to the oxygen atmosphere inside the Oxygen Delivery System (ODS), FDA UDI

Identifiers

Catalog Number
NA055-20 FDA UDI
Primary DI / UDI-DI
05060371000172 FDA UDI
510(k) Number
K112634 FDA UDI
FDA Product Code
KPJ FDA UDI
GMDN Term
Wound therapy oxygenator, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5650 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wound therapy oxygenator, single-use

NATROX® Oxygen Wound Therapy by Inotec Amd , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound therapy oxygenator, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Inotec Amd , Ltd.

Sources (1)

  • FDA UDI 3d8b0e07-0974-4cf8-87f1-990d56632701 37 fields · synced Jun 1, 2026