Primary Device ID | 10841522129292 |
NIH Device Record Key | 4f70c7f3-5903-427b-81c6-258d48b471ec |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SENTINEL |
Version Model Number | 98200 |
Catalog Number | 040-1723-01 |
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 | true |
Serial Number | false |
Manufacturing Date | true |
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 | 10841522129292 [Primary] |
DQK | Computer, diagnostic, programmable |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-10-10 |
Device Publish Date | 2022-09-30 |
10841522104565 | DISPLAY,19" LOW COST XPREZZON,94267 |
10841522123214 | SENTINEL 10 TEST SYSTEM HL7/DICOM |
10841522129315 | SENTINEL 11 / PATHFINDER SL KIT FR |
10841522129285 | SENTINEL 11 STANDALONE TEST SYSTEM |
10841522129551 | UPGRADE, SENTINEL 10.5 TO 11.5 OR HIGHER |
10841522129414 | SENTINEL 11 RDT TEST SYSTEM |
10841522129308 | SENTINEL 11 HL7 TEST SYSTEM |
10841522129292 | SENTINEL 11 NETWORKED TEST SYSTEM |
10841522104558 | 94267 |
10841522125751 | SENTINEL SOFTWARE V11 |
10841522130922 | SENTINEL 11 HL7 TEST SYSTEM |
10841522129384 | SENTINEL 11 / PATHFINDER SL KIT NL |
10841522129339 | SENTINEL 11 / PATHFINDER SL KIT IT |
10841522123207 | SENTINEL 10 TEST SYSTEM, RDT |
10841522123191 | SENTINEL 10 TEST SYSTEM, NETWORKED (ENG) |
10841522123184 | SENTINEL 10 TEST SYSTEM, STAND ALONE (ENG) |
10841522100710 | SENTINEL |