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LIFEPAK 20 and LIFEPAK 20e defibrillator/monitors

FDA UDI

by PHYSIO-CONTROL, Inc.

Identity

Trade Name
LIFEPAK 20 and LIFEPAK 20e defibrillator/monitors FDA UDI
Generic Name
Physiologic-monitoring defibrillation system FDA UDI
Device Name
PKG LP20E CMM,PCNG,SPO2,AHA USAS,ENG FDA UDI
Model / Reference
70507 FDA UDI
Description
PKG LP20E CMM,PCNG,SPO2,AHA USAS,ENG FDA UDI

Identifiers

Catalog Number
70507-000091 FDA UDI
Primary DI / UDI-DI
00883873813850 FDA UDI
GMDN Term
Physiologic-monitoring defibrillation system 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: Physiologic-monitoring defibrillation system

LIFEPAK 20 and LIFEPAK 20e defibrillator/monitors by PHYSIO-CONTROL, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Physiologic-monitoring defibrillation system.

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 071772f3-0c03-4a20-a0ce-0b660be9ad26 36 fields · synced Jun 9, 2026