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Masters Series™

FDA UDI

Class III (US FDA UDI)

by St. Jude Medical, Inc.

Identity

Trade Name
Masters Series™ FDA UDI
Generic Name
Mitral bi-leaflet mechanical heart valve prosthesis FDA UDI
Device Name
Mechanical Heart Valve FDA UDI
Model / Reference
31MECJ-502 FDA UDI
Description
Mechanical Heart Valve FDA UDI

Identifiers

Catalog Number
31MECJ-502 FDA UDI
Primary DI / UDI-DI
05415067045270 FDA UDI
FDA Product Code
LWQ FDA UDI
GMDN Term
Mitral 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 31.0000 Millimeter FDA UDI

Category: Mitral bi-leaflet mechanical heart valve prosthesis

Masters Series™ by St. Jude Medical, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
St. Jude Medical, Inc.

Sources (1)

  • FDA UDI a3d7d8d0-053f-461b-84d4-234a3d93ed70 36 fields · synced May 30, 2026