FDA UDI In Commercial Distribution 🇺🇸 United States

LIFEPAK® 1000 defibrillator

DI: 00883873869574 · Model: 97425 · PHYSIO-CONTROL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LIFEPAK® 1000 defibrillator
Primary DI
00883873869574
Version / Model
97425
Catalog Number
97425-000002
Company Name
PHYSIO-CONTROL, INC.
Labeler DUNS
009251992
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-04-10
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
6a505c1c-725a-4ff2-abc0-26fe3c86c4d8

Device Description

USED LP1000 UNIT1000AAAABAAACBAAAAAAAAAA

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
48049 Non-rechargeable professional semi-automated external defibrillator

Identifiers

Type ID
Primary 00883873869574

Customer Contacts