Primary Device ID | 06971679948976 |
NIH Device Record Key | c1a4a7c2-6b8c-41d2-91ce-00be80c99081 |
Commercial Distribution Discontinuation | 2025-08-05 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Shear Wave Quantificational Ultrasound Diagnostic System |
Version Model Number | Mini560 |
Company DUNS | 544348534 |
Company Name | Wuxi Hisky Medical Technologies Co.,Ltd. |
Device Count | 1 |
DM Exempt | true |
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 | 06971679948976 [Primary] |
IYN | System, Imaging, Pulsed Doppler, Ultrasonic |
Steralize Prior To Use | true |
Device Is Sterile | false |
[06971679948976]
Liquid Chemical
[06971679948976]
Liquid Chemical
[06971679948976]
Liquid Chemical
[06971679948976]
Liquid Chemical
[06971679948976]
Liquid Chemical
[06971679948976]
Liquid Chemical
[06971679948976]
Liquid Chemical
[06971679948976]
Liquid Chemical
[06971679948976]
Liquid Chemical
[06971679948976]
Liquid Chemical
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-08-13 |
Device Publish Date | 2025-08-05 |
06971679945005 | FT9000 |
06971679949072 | Mini800 |
06971679949065 | FT100 |
06971679949577 | Mini900 |
06971679948990 | Mini100 |
06971679948983 | Mini300 |
06971679948976 | Mini560 |
06971679948969 | Mini780 |
06971679948952 | Mini790 |
06971679948945 | Mini990 |