| Primary Device ID | 08809702986344 |
| NIH Device Record Key | e6443bf6-9f47-45c2-8b1e-0872f3d91b3d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LA3-14AD |
| Version Model Number | USP-L03EF5B/WR |
| 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 | 08809702986344 [Primary] |
| ITX | Transducer, Ultrasonic, Diagnostic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-12-24 |
| Device Publish Date | 2020-12-16 |
| 08800290027471 - EV2-12 | 2026-02-05 |
| 08800290041767 - EA2-11AV | 2026-02-05 |
| 08800290041811 - EA2-11AR | 2026-02-05 |
| 08800290042481 - PA2-9S | 2026-02-05 |
| 08800290042726 - CA2-13M | 2026-02-05 |
| 08800290065473 - EV2-12 | 2026-02-05 |
| 08800289975974 - R30 Diagnostic Ultrasound System | 2026-01-28 |
| 08800289976025 - R20 Diagnostic Ultrasound System | 2026-01-28 |