← Back to catalogue

LIFEPAK 1000 defibrillator

FDA UDI

Class III (US FDA UDI)

by PHYSIO-CONTROL, Inc.

Identity

Trade Name
LIFEPAK 1000 defibrillator FDA UDI
Generic Name
Non-rechargeable professional semi-automated external defibrillator FDA UDI
Device Name
LP1000 CONFIGURED UNIT1000AAAAAAAAAAAAAAAAAAAA FDA UDI
Model / Reference
99425 FDA UDI
Description
LP1000 CONFIGURED UNIT1000AAAAAAAAAAAAAAAAAAAA FDA UDI

Identifiers

Catalog Number
99425-000004 FDA UDI
Primary DI / UDI-DI
00883873815427 FDA UDI
PMA Number
P160026 FDA UDI
FDA Product Code
MKJ FDA UDI
GMDN Term
Non-rechargeable professional semi-automated external defibrillator 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Non-rechargeable professional semi-automated external defibrillator

LIFEPAK 1000 defibrillator by PHYSIO-CONTROL, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-rechargeable professional semi-automated external defibrillator.

Cleared under the same submission

P160026 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
PHYSIO-CONTROL, Inc.

Sources (1)

  • FDA UDI c2dbd712-f2d1-455f-87cc-c4e6a9e5900f 37 fields · synced Jun 9, 2026