DEVICE: OxySpur® lite Oxygen Diffusion Dressing (00851404004107)
Device Identifier (DI) Information
OxySpur® lite Oxygen Diffusion Dressing
2" x 8" Adhesive
In Commercial Distribution
600014
Electrochemical Oxygen Concepts, Inc.
2" x 8" Adhesive
In Commercial Distribution
600014
Electrochemical Oxygen Concepts, Inc.
OxySpur® lite Oxygen Diffusion Dressings are hydrophilic dressings designed for use with the OxyGeni® System in the management of wounds. The dressings are constructed with a non-adherent mesh layer directly adjacent to the wound, one lite absorbent hydrophilic foam layer with channels for oxygen distribution, covered by an occlusive film, and an adhesive border. The OxySpur® lite is to be used on wounds with minimal to low exudate, such as later in the wound healing cycle when wound exudate levels decrease.
Device Characteristics
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GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
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62348 | Wound therapy oxygenator dressing |
A sterile wound cover designed to be used in conjunction with a wound therapy oxygenator to actively promote continuous diffusion of oxygen (CDO) in a wound bed to heal various types of wounds (e.g., arterial, venous, diabetic or pressure ulcers, skin grafts, burns, and/or postoperative or traumatic wounds). It is made of synthetic polymer materials and consists of an absorbent open-cell foam layer, an oxygen (O2) distribution foam layer, an occlusive layer to create an O2 rich environment, and integrated O2 tubing/connector. It may have an adhesive border and may be cut to conform to the wound. O2 delivery extension tubing may be included. This is a single-use device.
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FDA Product Code
[?]Product Code | Product Code Name |
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KPJ | Chamber, Oxygen, Topical, Extremity |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
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K090681 | 000 |
Sterilization
Storage and Handling
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No storage/handling found |
Clinically Relevant Size
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No Device Sizes |
Device Record Status
5d2a31b8-fec3-4cdd-a000-a5bb1d3d62f6
August 01, 2023
1
July 24, 2023
August 01, 2023
1
July 24, 2023
Alternative and Additional Identifiers Additional Identifiers
Package DI
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Secondary DI
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No Secondary DIs found |
Unit of Use DI
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Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
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No Customer Contact currently defined