LIFEPAK CR2 AED Lithium Battery

FDA UDI

Class III (US FDA UDI)

by PHYSIO-CONTROL, Inc.

Identity

Trade Name: LIFEPAK CR2 AED Lithium Battery FDA UDI
Generic Name: Scalpel, single-use FDA UDI
Device Name: KIT, REPLACEMENT BATTERY, LPCR2, MULTI FDA UDI
Model / Reference: 11141 FDA UDI
Description: KIT, REPLACEMENT BATTERY, LPCR2, MULTI FDA UDI

Identifiers

Catalog Number: 11141-000165 FDA UDI
Primary DI / UDI-DI: 00883873867792 FDA UDI
FDA Product Code: MKJ FDA UDI
GMDN Term: Scalpel, single-use 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

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Scalpel, single-use

LIFEPAK CR2 AED Lithium 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 82b47d89-eeed-423c-a31b-beb423f1bc67 35 fields · synced Jun 9, 2026