Primary Device ID | 10841522125713 |
NIH Device Record Key | a8f37784-c2f9-41e8-8127-e2082f38c7aa |
Commercial Distribution Discontinuation | 2023-05-25 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | PathfinderSL |
Version Model Number | 98000 |
Catalog Number | 040-1754-00 |
Company DUNS | 145581588 |
Company Name | SPACELABS HEALTHCARE (WASHINGTON), 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 | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
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 | 10841522125713 [Primary] |
DQK | COMPUTER, DIAGNOSTIC, PROGRAMMABLE |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2024-05-08 |
Device Publish Date | 2018-08-03 |
10841522125638 | SENTINEL 10 / PATHFINDER SL KIT EN |
10841522125737 | SENTINEL 10 / PATHFINDER SL KIT DE |
10841522125720 | SENTINEL 10 / PATHFINDER SL KIT DN |
10841522125706 | SENTINEL 10 / PATHFINDER SL KIT BR-PT |
10841522125690 | SENTINEL 10 / PATHFINDER SL KIT PL |
10841522125683 | SENTINEL 10 / PATHFINDER SL KIT SV |
10841522125676 | SENTINEL 10 / PATHFINDER SL KIT ES |
10841522125669 | SENTINEL 10 / PATHFINDER SL KIT IT |
10841522125652 | SENTINEL 10 / PATHFINDER SL KIT FR |
10841522125102 | PATHFINDER SL KIT CN |
10841522124617 | CD ASSY PATHFINDER SL 1.9 |
10841522125713 | SENTINEL 10 / PATHFINDER SL KIT NL |