FDA UDI In Commercial Distribution 🇺🇸 United States

LIFEPAK 35 Monitor/Defibrillator

DI: 00883873765647 · Model: 70335 · PHYSIO-CONTROL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LIFEPAK 35 Monitor/Defibrillator
Primary DI
00883873765647
Version / Model
70335
Catalog Number
70335-000040
Company Name
PHYSIO-CONTROL, INC.
Labeler DUNS
009251992
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-29
Public Version
2
Public Version Date
2024-06-24
Public Version Status
Update
Public Device Record Key
302f859f-ef70-4ea1-9e17-77f0f6e344c7

Device Description

LP35,EN-US,MAS-SPO2,MED-CO2,SUN-NIBP,IP-TEMP,12L,WIFI/CELL/LN/CPRIN,STD

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
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
17882 Physiologic-monitoring defibrillation system

Identifiers

Type ID
Primary 00883873765647

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P160026 000