Aution™ Hybrid AU-4050 Chemical Analyzer
he AUTION HYBRID AU-4050 Fully Automated Integrated Urine Analyzer System contains a test strip chemistry urine analyzer and a flow cytometry urine particle analyzer together in a single…
he AUTION HYBRID AU-4050 Fully Automated Integrated Urine Analyzer System contains a test strip chemistry urine analyzer and a flow cytometry urine particle analyzer together in a single integrated device. The test strip chemistry module (CHM) is an automated urine analyzer intended for the in vitro measurement of the following parameters: glucose, protein, bilirubin, urobilinogen, pH, blood, ketones, nitrite, leukocytes, specific gravity, turbidity, and color. The chemistry module is intended for use with the Uriflet S 9HA multi-parameter urine chemistry test strips. The flow cytometry module (FCM) is an automated urine particle analyzer intended to analyze the following parameters in urine samples: Red Blood Cells, White Blood Cells, Epithelial Cells, Casts, and Bacteria and flags the presence of the following: Pathological Casts, Crystals, Sperm, Small Round Cells, Yeast Like Cells, and Mucus. The AUTION HYBRID AU-4050 is intended for in vitro diagnostic use in screening patient populations found in clinical laboratories.
Who Else Makes It
Concentrated in Jilin (4), Shandong (3), Zhejiang (2). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Acon Biotech (Hangzhou) Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 29 |
| Urit Medical Electronic Co., Ltd. | Guilin | Guangxi | Contract manufacturer | 28 |
| Dongguan Honfield Precision Parts Co., Ltd. | Zhangmutou, Dongguan | Guangdong | Contract manufacturer | 8 |
| Zhejiang Orient Gene Biotech | Huzhou | Zhejiang | Contract manufacturer | 86 |
| Dirui Industrial Co., Ltd. | Changchun | Jilin | Contract manufacturer | 84 |
| Infitek Co., Ltd. | Shanghai | Shanghai | Manufacturer | 49 |
| Labpeak Co., Ltd. | Jinan | Shandong | Manufacturer | 43 |
| Scitek Global Co., Ltd. | Jinan | Shandong | Manufacturer | 43 |
| Changchun Wancheng BIO-Electron Co., Ltd. | Changchun | Jilin | Contract manufacturer | 34 |
| Weihai Kangzheng Medical Equipments Technology Co., Ltd. | Weihai | Shandong | Contract manufacturer | 26 |
| Changchun Merydi BIO-Tech Co., Ltd. | Changchun | Jilin | Manufacturer | 24 |
| Jilin Hongyi BIO-Tech Co., Ltd. | Changchun | Jilin | Manufacturer | 24 |
Showing 12 of 16. All 16 manufacturers in China registered for Automated Urinalysis System
Record
| Listed by | Arkray USA, Inc., United States |
|---|---|
| FDA product code | KQO |
| Device type | Automated Urinalysis System |
| Device class | Class 1 |
| Regulation | 21 CFR 862.2900 |
| 510(k) | K121456 |
| Record published | 2017-02-06 |
| Record revised | 2022-09-16 (version 4) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Label carries | serial number |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 14603 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| iQ200 | Beckman Coulter Ireland Inc | 4 |
| Rapid Response | Btnx Inc. | 3 |
| Concentrated Washing Solution 3 | Arkray USA, Inc. | 2 |
| Aution™ Sticks 9EB – Test Strips | Arkray USA, Inc. | 2 |
| Clinitek Atlas® Control- Strips. | Siemens Healthcare Diagnostics Inc | 2 |
| My Yodoc | S-Connect Co., Ltd. | 2 |
| iChem Velocity | Beckman Coulter Ireland Inc | 2 |
| Mission U500 Urine Analyzer | Acon Laboratories, Inc. | 2 |
| Mission U120 Urine Analyzer | Acon Laboratories, Inc. | 2 |
| Aution EYE™ Control Solution H/L | Arkray USA, Inc. | 1 |
| Aution™ Diluent SED | Arkray USA, Inc. | 1 |
| DxU | Beckman Coulter, Inc. | 1 |
Showing 12 of 48. All products under Automated Urinalysis System
Recalls Naming This Product
1 recall names this product by its own identifier, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|---|---|
| Arkray Factory USA, Inc. | 510(k) number | 2019-05-03 | Class II | Software design | This correction is being initiated due to a software issue which results in the possibility of incorrect patient information being assigned to sample results when the following rare combination of three specific events were to occur: 1) No | 159 units | 2020-09-17 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.