Zoll Battery Li-Ion

FDA UDI

Class III (US FDA UDI)

by Zoll Medical Corporation

Identity

Trade Name: ZOLL BATTERY LI-ION FDA UDI
Generic Name: Portable/mobile rechargeable battery pack FDA UDI
Device Name: BATTERY, LI-ION 9 CELL 18650, RECONDITIONED FDA UDI
Model / Reference: 1009-001535-03-R FDA UDI
Description: BATTERY, LI-ION 9 CELL 18650, RECONDITIONED FDA UDI

Identifiers

Primary DI / UDI-DI: 00847946049898 FDA UDI
FDA Product Code: MKJ FDA UDI
GMDN Term: Portable/mobile rechargeable battery pack 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Portable/mobile rechargeable battery pack

Zoll Battery Li-Ion by Zoll Medical Corporation — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class III	Pending data

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Manufacturer

Manufacturer: Zoll Medical Corporation

Sources (1)

FDA UDI cd0233a9-ceee-4387-9802-1b2989b9845f 34 fields · synced Jun 8, 2026