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ASSURE, Carry Pack

FDA UDI

Class III (US FDA UDI)

by Kestra Medical Technologies, Inc.

Identity

Trade Name
ASSURE, Carry Pack FDA UDI
Generic Name
Wearable defibrillation system defibrillator FDA UDI
Device Name
A portable case that holds the Monitor while wearing the ASSURE system FDA UDI
Model / Reference
3326502-003 FDA UDI
Description
A portable case that holds the Monitor while wearing the ASSURE system FDA UDI

Identifiers

Catalog Number
3326502-003 FDA UDI
Primary DI / UDI-DI
00840241600207 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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: Wearable defibrillation system defibrillator

ASSURE, Carry Pack 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 0e4922eb-cb03-4be0-9f04-5c4199bd299d 36 fields · synced Jun 9, 2026