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X Series Monitor/Defibrillator

FDA UDI

Class III (US FDA UDI)

by Zoll Medical Corporation

Identity

Trade Name
X SERIES MONITOR/DEFIBRILLATOR FDA UDI
Generic Name
Noninvasive device battery charger FDA UDI
Device Name
X SERIES MONITOR/DEFIBRILLATOR, 3/5 LEAD, SPO2, NIBP, TEMP, CPR EXPANSION PACK, ETCO2, DMST FDA UDI
Model / Reference
610-0121411-01 FDA UDI
Description
X SERIES MONITOR/DEFIBRILLATOR, 3/5 LEAD, SPO2, NIBP, TEMP, CPR EXPANSION PACK, ETCO2, DMST FDA UDI

Identifiers

Primary DI / UDI-DI
00847946045470 FDA UDI
FDA Product Code
MKJ FDA UDI
GMDN Term
Noninvasive device battery charger FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
870.5310 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Electrocardiographic electrode, single-useRechargeable professional automated external defibrillatorBlood pressure cuff, single-useNoninvasive device battery charger

X Series Monitor/Defibrillator by Zoll Medical Corporation — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External defibrillation electrode, paediatric, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zoll Medical Corporation

Sources (1)

  • FDA UDI 8b419cc1-1beb-415c-94ab-0e3819d5647e 34 fields · synced Jun 8, 2026