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Open Pivot™

FDA UDI

Class III (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
Open Pivot™ FDA UDI
Generic Name
Aortic bi-leaflet mechanical heart valve prosthesis FDA UDI
Device Name
MHV 501DA20 AP AORTIC FDA UDI
Model / Reference
501DA20 FDA UDI
Description
MHV 501DA20 AP AORTIC FDA UDI

Identifiers

Primary DI / UDI-DI
00643169334885 FDA UDI
PMA Number
P990046 FDA UDI
FDA Product Code
LWQ FDA UDI
GMDN Term
Aortic bi-leaflet mechanical heart valve prosthesis 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

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Aortic bi-leaflet mechanical heart valve prosthesis

Open Pivot™ by Medtronic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Aortic bi-leaflet mechanical heart valve prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI 677ffca4-68b8-45c1-8eb6-f8178b8f3e8a 37 fields · synced May 30, 2026