Primary Device ID | 00859433006024 |
NIH Device Record Key | 1a5031b8-9df4-4849-b5f3-65c3a9843abd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | QuantaFlo |
Version Model Number | 91-0010 |
Company DUNS | 968030333 |
Company Name | SEMLER SCIENTIFIC, 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 | 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 | 00859433006024 [Primary] |
JOM | Plethysmograph, Photoelectric, Pneumatic Or Hydraulic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-08-19 |
00859433006123 | Software Application |
00859433006079 | USB Sensor, Tracking, Bard |
00859433006062 | USB Sensor, Tracking |
00859433006048 | Application |
00859433006024 | USB Sensor |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
QUANTAFLO 88274741 5827470 Live/Registered |
Semler Scientific, Inc. 2019-01-24 |