Primary Device ID | 00883873940204 |
NIH Device Record Key | 8fc666ff-968e-462f-984b-ffdaeb60d315 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 11140 |
Catalog Number | 11140-000072 |
Company DUNS | 009251992 |
Company Name | PHYSIO-CONTROL, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00883873940204 [Primary] |
MPD | Auxiliary power supply (AC or DC) for low-energy dc-defibrillator |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-05-08 |
Device Publish Date | 2019-04-30 |
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00883873765630 - LIFEPAK 35 Monitor/Defibrillator | 2024-07-08 LP35,EN-US,MAS-SPO2,MED-CO2,SUN-NIBP,IP-TEMP,12L,WIFI/CELL/L |
00883873765661 - LIFEPAK 35 Monitor/Defibrillator | 2024-07-08 LP35,EN-US,MAS-SP/CO,MED-CO2,SUN-NIBP,IP-TEMP,12L,WIFI/CELL |
00883873766255 - LIFEPAK 35 Monitor/Defibrillator | 2024-07-08 LP35,EN-US,MAS-SP/CO/MET,MED-CO2,SUN-NIBP,12L,WIFI/CELL/LN/C |
00883873772652 - LIFEPAK 35 Monitor/Defibrillator | 2024-07-08 LP35,EN-US,MAS-SP/CO/MET,MED-CO2,SUN-NIBP,IP-TEMP,12L,WIFI/C |
00883873765609 - LIFEPAK 35 Monitor/Defibrillator | 2024-07-05 LP35,EN-US,MAS-SP/CO,MED-CO2,SUN-NIBP,12L,WIFI/CELL/LN/CPRIN |