Primary Device ID | 00883873869468 |
NIH Device Record Key | a034b796-1206-4d08-b931-c038e334bee4 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 21300 |
Catalog Number | 21300-008146 |
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 | false |
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 |
Phone | +1(800)442-1142 |
rs.seacustomersupport@stryker.com | |
Phone | +1(800)442-1142 |
rs.seacustomersupport@stryker.com | |
Phone | +1(800)442-1142 |
rs.seacustomersupport@stryker.com | |
Phone | +1(800)442-1142 |
rs.seacustomersupport@stryker.com |
Length | 12 Feet |
Length | 12 Feet |
Length | 12 Feet |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00883873869468 [Primary] |
DSK | COMPUTER, BLOOD-PRESSURE |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-07-22 |
Device Publish Date | 2018-10-04 |
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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 |
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