FDA UDI Not in Commercial Distribution 🇺🇸 United States

LIFEPAK® 500 Automated External Defibrillator

DI: 00681490577533 · Model: 99401 · PHYSIO-CONTROL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LIFEPAK® 500 Automated External Defibrillator
Primary DI
00681490577533
Version / Model
99401
Catalog Number
99401-000150
Company Name
PHYSIO-CONTROL, INC.
Labeler DUNS
009251992
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-11-11
Public Version
3
Public Version Date
2019-05-30
Public Version Status
Update
Public Device Record Key
3e7b1591-da2a-4923-8d26-87b13c746f5d
Distribution End Date
2015-02-09

Device Description

FINAL ASSY-LP500,ENGLISHNO VOICE,2 BUTTON OP

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MKJ Automated external defibrillators (non-wearable)

GMDN Terms

Code Name
47910 Non-rechargeable public semi-automated external defibrillator

Identifiers

Type ID
Primary 00681490577533

Customer Contacts