Primary Device ID | 10841522128820 |
NIH Device Record Key | 455b046a-ad7d-443c-82d3-530e7029c8d7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pathfinder SL |
Version Model Number | Pathfinder SL |
Catalog Number | 040-1763-00 |
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 | 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 | 10841522128820 [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 | 2 |
Public Version Date | 2023-10-05 |
Device Publish Date | 2019-10-09 |
10841522126000 | PATHFINDER SL HOLTER ANALYSIS SYSTEM (ENGLISH) |
10841522128820 | INSTALLATION KIT, PATHFINDER SL 1.9.2 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PATHFINDER SL 85909266 4443589 Live/Registered |
SPACELABS HOLDINGS, INC. 2013-04-19 |