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Mitroflow Valsalva Conduit

FDA UDI

Class III (US FDA UDI)

by Corcym Canada Corp

Identity

Trade Name
MITROFLOW VALSALVA CONDUIT FDA UDI
Generic Name
Aortic open-surgery heart valve bioprosthesis/synthetic polymer aorta graft FDA UDI
Model / Reference
MVC FDA UDI

Identifiers

Primary DI / UDI-DI
08022057014955 FDA UDI
PMA Number
P060038 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
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
MRI Safety
MR Conditional FDA UDI

Category: Aortic open-surgery heart valve bioprosthesis/synthetic polymer aorta graft

Mitroflow Valsalva Conduit by Corcym Canada Corp — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Aortic open-surgery heart valve bioprosthesis/synthetic polymer aorta graft.

Cleared under the same submission

P060038 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Corcym Canada Corp

Sources (1)

  • FDA UDI 8f152734-39b0-4077-8eea-e911793bc217 33 fields · synced May 30, 2026