FDA UDI In Commercial Distribution 🇺🇸 United States

LIFEPAK® 20 and LIFEPAK 20e defibrillator/monitors

DI: 00883873887707 · Model: 99507 · 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
00883873887707
Version / Model
99507
Catalog Number
99507-000102
Company Name
PHYSIO-CONTROL, INC.
Labeler DUNS
009251992
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-10-20
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
fbe81fb5-62ed-486f-bd5c-ae2149da3e7c

Device Description

LP20E CONFIGURED - CMM,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 00883873887707

Customer Contacts