| Primary Device ID | 08809521021578 |
| NIH Device Record Key | 691d59ec-193c-4b34-964c-c6efaea1c51c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | HS40 Diagnostic Ultrasound System |
| Version Model Number | USS-HS4NL3C/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 | 08809521021578 [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 |