FDA UDI Not in Commercial Distribution 🇺🇸 United States

LIFEPAK® CR Plus and LIFEPAK Express defibrillators

DI: 00721902508196 · Model: 80403 · PHYSIO-CONTROL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LIFEPAK® CR Plus and LIFEPAK Express defibrillators
Primary DI
00721902508196
Version / Model
80403
Catalog Number
80403-000025
Company Name
PHYSIO-CONTROL, INC.
Labeler DUNS
009251992
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-11-14
Public Version
3
Public Version Date
2019-05-01
Public Version Status
Update
Public Device Record Key
ad70deb4-6c3f-4bbd-a7b8-f943dcb94c46
Distribution End Date
2019-04-30

Device Description

PACKAGE,LP CR PLUS,AUTO,PULSE

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
Yes
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
48045 Rechargeable public semi-automated external defibrillator

Identifiers

Type ID
Primary 00721902508196

Customer Contacts