DEVICE: CARDINAL HEALTH (00888499001346)
Device Identifier (DI) Information
CARDINAL HEALTH
WC8OZ
In Commercial Distribution
WC8OZ
Cardinal Health 200, LLC
WC8OZ
In Commercial Distribution
WC8OZ
Cardinal Health 200, LLC
Wound Cleanser
No-rinse, non-irritating formulation
Non-ionic surfactant
Directions for use:
1. Turn nozzle to stream or spray position.
2. Spray contents on area to be cleansed approximately 3 inches away.
Ingredients: Purified water, poloxamer 188, sodium bicarbonate, sorbitol, citric acid, disodium EDTA, methylparaben, imidazolidinyl urea
Indications: May be used for the removal of foreign materials such as dirt and debris from dermal wounds.
Caution: For external use only. Keep this and all similar products out of the reach of children.
Store at ambient temperature.
Device Characteristics
Labeling does not contain MRI Safety Information | |
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No |
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? |
---|---|---|---|---|
47156 | Skin detergent |
A non-dedicated chemical solution intended to be applied to the surface of the skin for cleaning and/or conditioning, and is commonly used to remove dirt, debris, peeling skin, and/or for the attenuation of minor skin disorders (e.g., dry skin). It contains a synthetic surfactant (e.g., sodium laureth sulfate) and is normally available [non-prescription] over-the-counter (OTC) for home-use. After application, this device cannot be reused.
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Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
FRO | Dressing, wound, drug |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
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Premarket Submission Number Not Available/Not Released |
Sterilization
Storage and Handling
[?]Storage and Handling |
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No storage/handling found |
Clinically Relevant Size
[?]Size Type Text |
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No Device Sizes |
Device Record Status
47015e04-1b1a-4a5f-8ffa-736090823755
January 25, 2024
2
May 16, 2019
January 25, 2024
2
May 16, 2019
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
---|---|---|---|---|---|
10888499001343 | 12 | 00888499001346 | 2025-11-20 | In Commercial Distribution | CASE |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
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No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
00885380171867
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
No Customer Contact currently defined