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HeartMate™

FDA UDI

Class III (US FDA UDI)

by Thoratec Corp

Identity

Trade Name
HeartMate™ FDA UDI
Generic Name
Personal device holder, reusable FDA UDI
Device Name
Travel Bag FDA UDI
Model / Reference
1260 FDA UDI
Description
Travel Bag FDA UDI

Identifiers

Catalog Number
1260 FDA UDI
Primary DI / UDI-DI
05415067039606 FDA UDI
PMA Number
P160054 FDA UDI
FDA Product Code
DSQ FDA UDI
GMDN Term
Personal device holder, reusable FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Personal device holder, reusable

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

Similar devices

Also classified as Personal device holder, reusable.

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 cc24a9d4-0dc7-42d1-8f42-a1da217f41fb 37 fields · synced Jun 6, 2026