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ASSURE, Tablet

FDA UDI

Class III (US FDA UDI)

by Kestra Medical Technologies, Inc.

Identity

Trade Name
ASSURE, Tablet FDA UDI
Generic Name
Wearable defibrillation system defibrillator FDA UDI
Device Name
An electronic device used to program the ASSURE system and assist in patient fitting and training FDA UDI
Model / Reference
80041-001 FDA UDI
Description
An electronic device used to program the ASSURE system and assist in patient fitting and training FDA UDI

Identifiers

Catalog Number
80041-001 FDA UDI
Primary DI / UDI-DI
00840241600191 FDA UDI
PMA Number
P200037 FDA UDI
FDA Product Code
MVK FDA UDI
GMDN Term
Wearable defibrillation system defibrillator 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Wearable defibrillation system defibrillator

ASSURE, Tablet by Kestra Medical Technologies, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wearable defibrillation system defibrillator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0999c4d5-a79b-4d39-8491-0b11f76dfca3 36 fields · synced Jun 9, 2026