DEVICE: PERCEVAL (08022057014702)
Device Identifier (DI) Information
Device Characteristics
MR Conditional | |
No | |
No | |
Yes | |
Yes | |
No | |
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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? |
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60242 | Aortic open-surgery heart valve bioprosthesis |
A xenograft (e.g., porcine or bovine heart valve) intended to be implanted in a patient during open heart surgery to repair or replace a dysfunctional aortic heart valve. It is processed to render the tissue in the valve non-viable; it may be tissue only, or tissue attached to a metal or synthetic polymer framework. The device is typically used to treat acquired or congenital valvular disease.
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Active | true |
FDA Product Code
[?]Product Code | Product Code Name |
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LWR | Heart-Valve, Non-Allograft Tissue |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
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P150011 | 028 |
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
a7a4166c-ea20-4343-baea-4ee54d0ac17b
May 22, 2025
2
May 09, 2025
May 22, 2025
2
May 09, 2025
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
[?]
No Customer Contact currently defined