Primary Device ID | 08809521021776 |
NIH Device Record Key | e63e83a1-8453-4b83-96dc-93f4ea90462b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HS40 Diagnostic Ultrasound System |
Version Model Number | USS-HS4PB3C/US |
Company DUNS | 687785691 |
Company Name | SAMSUNG MEDISON CO., LTD. |
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 | 08809521021776 [Primary] |
ITX | Transducer, Ultrasonic, Diagnostic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-01-10 |
Device Publish Date | 2019-06-21 |
08809521021974 | USS-HS4PF3C/US |
08809521021776 | USS-HS4PB3C/US |
08809521021578 | USS-HS4NL3C/US |
08809521021219 | USS-HS4NB3C/US |
08809521021172 | USS-HS4PF4C/US |
08809521021165 | USS-HS4PB4C/US |
08809521020960 | USS-HS4NL4C/US |
08809521020762 | USS-HS4NB4C/US |
08806167791056 | USS-HS4NL3B/US |
08806167790837 | USS-HS4PF3B/US |
08806167790790 | USS-HS4PF4B/US |
08806167790646 | USS-HS4NL4B/US |
08809702984593 | USS-HS4PF3D/US |
08809702984395 | USS-HS4PB3D/US |
08809702984197 | USS-HS4NL3D/US |
08809702983831 | USS-HS4NB3D/US |
08809702983794 | USS-HS4PF4D/US |
08809702983787 | USS-HS4PB4D/US |
08809702983589 | USS-HS4NL4D/US |
08809702983381 | USS-HS4NB4D/US |
08806167783327 | USS-HS4PF30/US |
08806167782948 | USS-HS4NL30/US |