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LIFEPAK® 20 and LIFEPAK 20e defibrillator/monitors

FDA UDI

Class III (US 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
LP20E PACKAGE - CMM, PACING, SPO2, ENGLISH FDA UDI
Model / Reference
70507 FDA UDI
Description
LP20E PACKAGE - CMM, PACING, SPO2, ENGLISH FDA UDI

Identifiers

Catalog Number
70507-000091 FDA UDI
Primary DI / UDI-DI
00885074852133 FDA UDI
FDA Product Code
MKJ FDA UDI
GMDN Term
Physiologic-monitoring defibrillation system FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
870.5310 FDA UDI
Commercial Distribution
Not 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

No

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

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

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

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 71aee3e7-2481-4293-9f30-48d2c4807362 36 fields · synced Jun 9, 2026