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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
USED LP1000 UNIT1000AAAABAAACBAAAAAAAAAA FDA UDI
Model / Reference
97425 FDA UDI
Description
USED LP1000 UNIT1000AAAABAAACBAAAAAAAAAA FDA UDI

Identifiers

Catalog Number
97425-000002 FDA UDI
Primary DI / UDI-DI
00883873869574 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

Yes

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.

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 6a505c1c-725a-4ff2-abc0-26fe3c86c4d8 35 fields · synced Jun 9, 2026