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AutoPulse NXT Multi-Chemistry Battery Charger

FDA UDI

Class II (US FDA UDI)

by ZOLL Circulation, Inc.

Identity

Trade Name
AutoPulse NXT Multi-Chemistry Battery Charger FDA UDI
Generic Name
Cardiac resuscitator, line-powered FDA UDI
Device Name
The AutoPulse NXT System consists of 4 primary components, a reusable Platform, a single use chest compression assembly (LifeBand), a rechargeable battery, and a battery charger. FDA UDI
Model / Reference
Model 200 FDA UDI
Description
The AutoPulse NXT System consists of 4 primary components, a reusable Platform, a single use chest compression assembly (LifeBand), a rechargeable battery, and a battery charger. FDA UDI

Identifiers

Catalog Number
8700-001071 FDA UDI
Primary DI / UDI-DI
00849111003568 FDA UDI
FDA Product Code
DRM FDA UDI
GMDN Term
Cardiac resuscitator, line-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5200 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: Cardiac resuscitator, line-powered

AutoPulse NXT Multi-Chemistry Battery Charger by ZOLL Circulation, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiac resuscitator, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e3fa2485-a5fc-4253-b9b8-ce489b8d6608 36 fields · synced Jun 9, 2026