← Back to catalogue

LIFEPAK 15 monitor/defibrillator

FDA UDI

by PHYSIO-CONTROL, Inc.

Identity

Trade Name
LIFEPAK 15 monitor/defibrillator FDA UDI
Generic Name
Electrocardiographic lead set, reusable FDA UDI
Device Name
LP15 ACCRY SHIPKIT,AHA,S FDA UDI
Model / Reference
41577 FDA UDI
Description
LP15 ACCRY SHIPKIT,AHA,S FDA UDI

Identifiers

Catalog Number
41577-000267 FDA UDI
Primary DI / UDI-DI
00883873870440 FDA UDI
GMDN Term
Electrocardiographic lead set, reusable 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrocardiographic lead set, reusableBlood pressure cuff, reusableGeneral-purpose patient temperature probe, reusable

LIFEPAK 15 monitor/defibrillator by PHYSIO-CONTROL, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose patient temperature probe, reusable.

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 e26a82d8-9cba-4b44-8570-38d3e6583f0a 35 fields · synced Jun 9, 2026