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OxyGeni® Oxygen Delivery Extension Set

FDA UDI

Class II (US FDA UDI)

by Electrochemical Oxygen Concepts, Inc.

Identity

Trade Name
OxyGeni® Oxygen Delivery Extension Set FDA UDI
Generic Name
Wound therapy oxygenator tubing FDA UDI
Device Name
The OxyGeni® Oxygen Delivery Extension Set is an optional accessory of the OxyGeni® System. It is a length of flexible tubing extension with connectors at both ends intended to connect the OxyGeni® Oxygen Generator to the proprietary Oxygen Diffusion Dressings to deliver oxygen (O2) to a wound bed during continuous diffusion of oxygen (CDO™) therapy. It may be secured to the skin using medical tape. FDA UDI
Model / Reference
620000 FDA UDI
Description
The OxyGeni® Oxygen Delivery Extension Set is an optional accessory of the OxyGeni® System. It is a length of flexible tubing extension with connectors at both ends intended to connect the OxyGeni® Oxygen Generator to the proprietary Oxygen Diffusion Dressings to deliver oxygen (O2) to a wound bed during continuous diffusion of oxygen (CDO™) therapy. It may be secured to the skin using medical tape. FDA UDI

Identifiers

Primary DI / UDI-DI
00851404004114 FDA UDI
510(k) Number
K090681 FDA UDI
FDA Product Code
KPJ FDA UDI
GMDN Term
Wound therapy oxygenator tubing 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

No

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
MRI Safety
MR Conditional FDA UDI

Category: Wound therapy oxygenator tubing

OxyGeni® Oxygen Delivery Extension Set by Electrochemical Oxygen Concepts, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound therapy oxygenator tubing.

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 9173fc55-2d65-45f2-b44a-baa33342ae71 35 fields · synced Jun 6, 2026