DEVICE: Medical Action Industries (10809160293300)
Device Identifier (DI) Information
Medical Action Industries
79832
Not in Commercial Distribution
MEDICAL ACTION INDUSTRIES INC.
79832
Not in Commercial Distribution
MEDICAL ACTION INDUSTRIES INC.
No description.
Device Characteristics
Labeling does not contain MRI Safety Information | |
No | |
Yes | |
Yes | |
No | |
Yes | |
Yes | |
No | |
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? |
---|---|---|---|---|
17983 | Infectious waste spill kit |
A set of devices used to clean up spillage of infectious material. It provides equipment and material for an appropriate method for removing the spillage, and includes the proper container for the disposal of the spillage. This is a single-use device.
|
Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
OKG | Body fluid clean up kit |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
---|---|
Premarket Submission Number Not Available/Not Released |
Sterilization
Storage and Handling
[?]Storage and Handling |
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Special Storage Condition, Specify: STORE AT ROOM TEMPERATURE |
Special Storage Condition, Specify: |
Clinically Relevant Size
[?]Size Type Text |
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No Device Sizes |
Device Record Status
589301b0-e61d-436c-b25b-3dd71d2b8ba6
January 18, 2023
2
October 05, 2020
January 18, 2023
2
October 05, 2020
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
---|---|---|---|---|---|
20809160293307 | 20 | 10809160293300 | 2023-01-17 | Not in Commercial Distribution |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
---|---|
No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
No Customer Contact currently defined