FDA UDI Not in Commercial Distribution 🇺🇸 United States

LIFEPAK® 20 and LIFEPAK 20e defibrillator/monitors

DI: 00721902505461 · Model: 99402 · PHYSIO-CONTROL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LIFEPAK® 20 and LIFEPAK 20e defibrillator/monitors
Primary DI
00721902505461
Version / Model
99402
Catalog Number
99402-000033
Company Name
PHYSIO-CONTROL, INC.
Labeler DUNS
009251992
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-11-05
Public Version
3
Public Version Date
2019-05-01
Public Version Status
Update
Public Device Record Key
4ea8f7f7-d95c-4a99-8d51-39e950985b2b
Distribution End Date
2019-04-30

Device Description

LP20-CONFIGURED,W/PACING,SPO2,ENGLISH

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
17882 Physiologic-monitoring defibrillation system

Identifiers

Type ID
Primary 00721902505461

Customer Contacts