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HeartMate 3™

FDA UDI

Class III (US FDA UDI)

by Thoratec Corp

Identity

Trade Name
HeartMate 3™ FDA UDI
Generic Name
Implantable ventricular circulatory assist system FDA UDI
Device Name
Apical Cuff FDA UDI
Model / Reference
106522US FDA UDI
Description
Apical Cuff FDA UDI

Identifiers

Catalog Number
106522US FDA UDI
Primary DI / UDI-DI
05415067039286 FDA UDI
PMA Number
P160054 FDA UDI
FDA Product Code
DSQ FDA UDI
GMDN Term
Implantable ventricular circulatory assist system 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
MRI Safety
MR Unsafe FDA UDI

Category: Implantable ventricular circulatory assist system

HeartMate 3™ by Thoratec Corp — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Implantable ventricular circulatory assist system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Thoratec Corp

Sources (1)

  • FDA UDI 4c807daf-27b4-4db0-8ebe-e552dbb13f4b 37 fields · synced Jun 8, 2026