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LIFEPAK CR Plus and LIFEPAK Express defibrillators

FDA UDI

by PHYSIO-CONTROL, Inc.

Identity

Trade Name
LIFEPAK CR Plus and LIFEPAK Express defibrillators FDA UDI
Generic Name
Rechargeable public semi-automated external defibrillator FDA UDI
Device Name
PACKAGE,LP CR PLUS,SEMI,PULSE FDA UDI
Model / Reference
80403 FDA UDI
Description
PACKAGE,LP CR PLUS,SEMI,PULSE FDA UDI

Identifiers

Catalog Number
80403-000002 FDA UDI
Primary DI / UDI-DI
00883873820407 FDA UDI
GMDN Term
Rechargeable public semi-automated external defibrillator FDA UDI

Classification

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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Rechargeable public semi-automated external defibrillator

LIFEPAK CR Plus and LIFEPAK Express defibrillators by PHYSIO-CONTROL, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rechargeable public semi-automated external defibrillator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
PHYSIO-CONTROL, Inc.

Sources (1)

  • FDA UDI e838182a-1d89-4958-aaab-d0a63ce09994 36 fields · synced Jun 9, 2026