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Thoratec® Pvad™, Ventricular Assist Device - Blood Pump

FDA UDI

Class III (US FDA UDI)

by Thoratec Corp

Identity

Trade Name
THORATEC® PVAD™, VENTRICULAR ASSIST DEVICE - BLOOD PUMP FDA UDI
Generic Name
External ventricular circulatory assist system FDA UDI
Device Name
VAD, STERILE, CLINICAL FDA UDI
Model / Reference
14086-2550-000 FDA UDI
Description
VAD, STERILE, CLINICAL FDA UDI

Identifiers

Catalog Number
14086-2550-000 FDA UDI
Primary DI / UDI-DI
00813024012009 FDA UDI
FDA Product Code
DSQ FDA UDI
GMDN Term
External 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

No

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

Yes

FDA UDI

Category: External ventricular circulatory assist system

Thoratec® Pvad™, Ventricular Assist Device - Blood Pump by Thoratec Corp — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External ventricular circulatory assist system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Thoratec Corp

Sources (1)

  • FDA UDI 494aac8f-db6f-4047-9b46-b5491102e4d1 36 fields · synced May 30, 2026