Primary Device ID | 08809880022438 |
NIH Device Record Key | 8592c274-c073-4be4-9f4b-89dddbca93af |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HS40 |
Version Model Number | USS-HS4NG3F/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 | 08809880022438 [Primary] |
IYN | System, Imaging, Pulsed Doppler, Ultrasonic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-09-02 |
Device Publish Date | 2022-08-25 |
08809725785962 | USS-HS4NB3E/US |
08809725787027 | USS-HS4NF3E/US |
08809725785740 | USS-HS4NF4E/US |
08809725785221 | USS-HS4NL4E/US |
08809725785023 | USS-HS4NB4E/US |
08809880022933 | USS-HS4PB4F/US |
08809880022766 | USS-HS4PB3F/US |
08809880022605 | USS-HS4NG4F/US |
08809880022438 | USS-HS4NG3F/US |
08809880022261 | USS-HS4NB4F/US |
08809880022094 | USS-HS4PF4F/US |
08809880021929 | USS-HS4PF3F/US |
08809880021745 | USS-HS4NL4F/US |
08809880021578 | USS-HS4NL3F/US |
08809880021400 | USS-HS4NF4F/US |
08809880021233 | USS-HS4NF3F/US |
08809880021066 | USS-HS4NB3F/US |