FDA UDI In Commercial Distribution 🇺🇸 United States

LIFEPAK® 12 defibrillator/monitor

DI: 00885074318929 · Model: 99400 · PHYSIO-CONTROL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LIFEPAK® 12 defibrillator/monitor
Primary DI
00885074318929
Version / Model
99400
Catalog Number
99400-002984
Company Name
PHYSIO-CONTROL, INC.
Labeler DUNS
009251992
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-11-05
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
341aa9ba-475a-4231-b023-e01f267bd0c7

Device Description

LP12AOBCAAAACBABAAAAAAAALP12 MONITOR-DEFIB

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 00885074318929

Customer Contacts