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ASSURE, Battery

FDA UDI

Class III (US FDA UDI)

by Kestra Medical Technologies, Inc.

Identity

Trade Name
ASSURE, Battery FDA UDI
Generic Name
Wearable defibrillation system defibrillator FDA UDI
Device Name
A rechargeable battery that powers the ASSURE System FDA UDI
Model / Reference
3322882-005 FDA UDI
Description
A rechargeable battery that powers the ASSURE System FDA UDI

Identifiers

Catalog Number
3322882-005 FDA UDI
Primary DI / UDI-DI
00840241600009 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, Battery 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 09504411-2a48-4b88-8b8b-2dc12094845c 37 fields · synced Jun 9, 2026