Identity
- Trade Name
- MITROFLOW VALSALVA CONDUIT FDA UDI
- Generic Name
- Aortic open-surgery heart valve bioprosthesis/synthetic polymer aorta graft FDA UDI
- Model / Reference
- MVC26 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08022057014924 FDA UDI
- FDA Product Code
- LWR FDA UDI
- GMDN Term
- Aortic open-surgery heart valve bioprosthesis/synthetic polymer aorta graft FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Mitroflow Valsalva Conduit by Corcym Canada Corp — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class III | Pending data |
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Manufacturer
- Manufacturer
- Corcym Canada Corp
Sources (1)
- FDA UDI c61e4958-b445-4cd3-b0c4-3e91c521d1c6 33 fields · synced Jun 8, 2026