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ASSURE, Monitor

FDA UDI

Class III (US FDA UDI)

by Kestra Medical Technologies, Inc.

Identity

Trade Name
ASSURE, Monitor FDA UDI
Generic Name
Wearable defibrillation system defibrillator FDA UDI
Device Name
A part of the ASSURE System that provides power and displays system status information FDA UDI
Model / Reference
80008-003 FDA UDI
Description
A part of the ASSURE System that provides power and displays system status information FDA UDI

Identifiers

Catalog Number
80008-003 FDA UDI
Primary DI / UDI-DI
00840241600030 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
MRI Safety
MR Unsafe FDA UDI

Category: Wearable defibrillation system defibrillator

ASSURE, Monitor 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 6e3e421b-96e6-46bb-8ad1-b724113ab6b4 37 fields · synced Jun 9, 2026