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Tendyne™

FDA UDI

Class III (US FDA UDI)

by St. Jude Medical, Inc.

Identity

Trade Name
Tendyne™ FDA UDI
Generic Name
Mitral transcatheter heart valve bioprosthesis FDA UDI
Device Name
Pad Positioning System FDA UDI
Model / Reference
TENDV-PS FDA UDI
Description
Pad Positioning System FDA UDI

Identifiers

Catalog Number
TENDV-PS FDA UDI
Primary DI / UDI-DI
05415067032713 FDA UDI
PMA Number
P240042 FDA UDI
FDA Product Code
NPU FDA UDI
GMDN Term
Mitral transcatheter heart valve bioprosthesis 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Mitral transcatheter heart valve bioprosthesis

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

Similar devices

Also classified as Mitral transcatheter heart valve bioprosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6165fedc-bf40-44a4-8636-5755be775d8b 37 fields · synced May 30, 2026