LIFEPAK 500 DPS Li-SO2 Non-Rechargeable Battery

FDA UDI

Class III (US FDA UDI)

by PHYSIO-CONTROL, Inc.

Identity

Trade Name: LIFEPAK 500 DPS Li-SO2 Non-Rechargeable Battery FDA UDI
Generic Name: Primary battery FDA UDI
Device Name: ASSY-BATTERY,LITHIUM,4CELL,DSIZE,DARK GREY,MULT FDA UDI
Model / Reference: 11141 FDA UDI
Description: ASSY-BATTERY,LITHIUM,4CELL,DSIZE,DARK GREY,MULT FDA UDI

Identifiers

Catalog Number: 11141-000157 FDA UDI
Primary DI / UDI-DI: 00883873919446 FDA UDI
FDA Product Code: MKJ FDA UDI
GMDN Term: Primary battery 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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Primary battery

LIFEPAK 500 DPS Li-SO2 Non-Rechargeable Battery by PHYSIO-CONTROL, Inc. — 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: PHYSIO-CONTROL, Inc.

Sources (1)

FDA UDI b9579952-7b5c-4e01-8f3f-2fc9ac564585 35 fields · synced Jun 9, 2026