| Primary Device ID | 06971355420864 |
| NIH Device Record Key | 16da7924-0076-49b0-b312-5f180623d341 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Diagnostic Ultrasound System |
| Version Model Number | Clivia 90Elite |
| Company DUNS | 543063066 |
| Company Name | SHENZHEN WISONIC MEDICAL TECHNOLOGY CO., LTD. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| 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 | 06971355420864 [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 | 2022-02-04 |
| Device Publish Date | 2022-01-27 |
| 06971355420932 | Clivia 90Go |
| 06971355420925 | Clivia 90Plus |
| 06971355420918 | Clivia 90Pro |
| 06971355420901 | Clivia 90T |
| 06971355420895 | Clivia 90 |
| 06971355420888 | Clivia 90Nova |
| 06971355420871 | Clivia 90Exp |
| 06971355420864 | Clivia 90Elite |
| 06971355421335 | Carnation Fast |
| 06971355421328 | Carnation Ultra |
| 06971355421311 | Carnation Pro |
| 06971355421304 | Carnation T |
| 06971355421298 | Carnation |
| 06971355421281 | Carnation Neo |
| 06971355421274 | Carnation Exp |
| 06971355421267 | Carnation+ |