DEVICE: OC-Auto (00816917020334)
Device Identifier (DI) Information
OC-Auto
OCPU-KPS FT
In Commercial Distribution
POLYMEDCO CANCER DIAGNOSTIC PRODUCTS LLC
OCPU-KPS FT
In Commercial Distribution
POLYMEDCO CANCER DIAGNOSTIC PRODUCTS LLC
Personal Use Kit OC-Auto, for KPS Fontana
Device Characteristics
Labeling does not contain MRI Safety Information | |
No | |
No | |
Yes | |
No | |
No | |
No | |
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? |
---|---|---|---|---|
54533 | Faecal occult blood IVD, reagent |
A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative screening of stool (faeces) for occult blood (haemoglobin).
|
Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
OOX | Automated Occult Blood Analyzer |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
---|---|
K041408 | 000 |
Sterilization
Storage and Handling
[?]Storage and Handling |
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Handling Environment Temperature: between 2 and 30 Degrees Celsius |
Clinically Relevant Size
[?]Size Type Text |
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No Device Sizes |
Device Record Status
bec2c8ae-6304-437b-aa73-df3e1fecc053
October 24, 2018
1
September 23, 2018
October 24, 2018
1
September 23, 2018
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
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No Package DIs found |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
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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