Primary Device ID | 04987670100710 |
NIH Device Record Key | fe997f45-ac34-41f5-aec9-cd6a557393a4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DIAGNOSTIC ULTRASOUND SYSTEM |
Version Model Number | TUS-A400 |
Company DUNS | 690575113 |
Company Name | CANON MEDICAL SYSTEMS CORPORATION |
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 | false |
OTC Over-The-Counter | false |
Phone | +1-8004211968 |
xxx@xxx.xxx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04987670100710 [Primary] |
IYO | System, imaging, pulsed echo, ultrasonic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-01 |
04987670103469 | DIAGNOSTIC ULTRASOUND SYSTEM |
04987670103452 | DIAGNOSTIC ULTRASOUND SYSTEM |
04987670103353 | DIAGNOSTIC ULTRASOUND SYSTEM |
04987670103346 | DIAGNOSTIC ULTRASOUND SYSTEM |
04987670102981 | DIAGNOSTIC ULTRASOUND SYSTEM |
04987670102523 | DIAGNOSTIC ULTRASOUND SYSTEM |
04987670102516 | DIAGNOSTIC ULTRASOUND SYSTEM |
04987670102509 | DIAGNOSTIC ULTRASOUND SYSTEM |
04987670100765 | DIAGNOSTIC ULTRASOUND SYSTEM |
04987670100758 | DIAGNOSTIC ULTRASOUND SYSTEM |
04987670100741 | DIAGNOSTIC ULTRASOUND SYSTEM |
04987670100734 | DIAGNOSTIC ULTRASOUND SYSTEM |
04987670100727 | DIAGNOSTIC ULTRASOUND SYSTEM |
04987670100710 | DIAGNOSTIC ULTRASOUND SYSTEM |
04987670100703 | DIAGNOSTIC ULTRASOUND SYSTEM |
04987670103780 | CUS-AA000 |
04987670104558 | CUS-AGG00 |
04987670104541 | CUS-AFL00 |