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Thoratec® HeartMate 3™

FDA UDI

Class III (US FDA UDI)

by Thoratec Corp

Identity

Trade Name
Thoratec® HeartMate 3™ FDA UDI
Generic Name
Implantable ventricular circulatory assist system outflow cannula, animal-derived FDA UDI
Device Name
Sealed Outflow Graft with Bend Relief FDA UDI
Model / Reference
105581US FDA UDI
Description
Sealed Outflow Graft with Bend Relief FDA UDI

Identifiers

Catalog Number
105581US FDA UDI
Primary DI / UDI-DI
00813024013266 FDA UDI
FDA Product Code
DSQ FDA UDI
GMDN Term
Implantable ventricular circulatory assist system outflow cannula, animal-derived 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 outflow cannula, animal-derived

Thoratec® 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 outflow cannula, animal-derived.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Thoratec Corp

Sources (1)

  • FDA UDI 863115ce-cf41-497e-877d-0ddc84e6660c 36 fields · synced May 30, 2026