← Back to catalogue

Thoratec®, Hearttouch® Tablet Li-Ion Battery

FDA UDI

Class III (US FDA UDI)

by Thoratec Corp

Identity

Trade Name
THORATEC®, HEARTTOUCH® TABLET LI-ION BATTERY FDA UDI
Generic Name
Secondary battery FDA UDI
Model / Reference
105610 FDA UDI

Identifiers

Catalog Number
105610 FDA UDI
Primary DI / UDI-DI
00813024011798 FDA UDI
FDA Product Code
DSQ FDA UDI
GMDN Term
Secondary battery 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Secondary battery

Thoratec®, Hearttouch® Tablet Li-Ion Battery by Thoratec Corp — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Secondary battery.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Thoratec Corp

Sources (1)

  • FDA UDI 38b54ab5-c06b-42ea-bcbb-0c6ee7a0da2b 35 fields · synced May 30, 2026