Primary Device ID | 06971355421328 |
NIH Device Record Key | 1c9827f3-408a-48e6-bf60-2f1bfd764b7f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Diagnostic Ultrasound System |
Version Model Number | Carnation Ultra |
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 | 06971355421328 [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 | 2023-10-19 |
Device Publish Date | 2023-10-11 |
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+ |