Dimension Vista® Flex® Reagent Cartridge Ldlc
Low-Density Lipoprotein Cholesterol Flex® reagent cartridge, 180 Tests
3manufacturers in China registered for this device type
1catalogue number
1510(k) clearance
2recalls on this code
Who Else Makes It
Concentrated in Shandong (1), Guangxi (1), Hebei (1).
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Biobase Biodustry(Shandong)Co., Ltd. | Jinan | Shandong | Manufacturer | 70 |
| Urit Medical Electronic Co., Ltd. | Guilin | Guangxi | Contract manufacturer | 28 |
| Shijiazhuang Hipro Biotechnology Co., Ltd. | Shijiazhuang | Hebei | Manufacturer | 22 |
Record
| Listed by | Siemens Healthcare Diagnostics Inc, United States |
|---|---|
| FDA product code | MRR |
| Device type | System, Test, Low Density, Lipoprotein |
| Device class | Class 1 |
| Regulation | 21 CFR 862.1475 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| 510(k) | K061655 |
| Record published | 2020-09-24 |
| Record revised | 2023-07-06 (version 3) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Label carries | lot or batch number, expiry date |
| Storage | Storage environment temperature 2 to 8 °C |
Catalogue Numbers
| Catalogue number | Size | Per pack | Status |
|---|---|---|---|
| 10445096 | 2 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Biobase | Biobase Biodustry(Shandong)Co., Ltd. | 19 |
| Carolina Liquid Chemistries Corp.® LDL Cholesterol Direct Reagent KIT DT661 | Carolina Liquid Chemistries | 4 |
| Pointe Scientific, Inc. | Horiba Instruments Incorporated | 3 |
| Direct LDL-Cholesterol (LDL) | Randox Laboratories Limited | 3 |
| Pointe autoLDL Cholesterol Reagent | Horiba Instruments Incorporated | 2 |
| N-geneous LDL-ST Cholesterol Reagent (R1) | Sekisui Diagnostics, LLC | 2 |
| Mercodia Oxidized LDL Elisa | Mercodia AB | 2 |
| ACE | Alfa Wassermann | 2 |
| N-geneous LDL-ST Cholesterol Reagent (R2) | Sekisui Diagnostics, LLC | 2 |
| Advia® Chemistry Direct LDL Cholesterol Reagents | Siemens Healthcare Diagnostics Inc | 1 |
| MedTest Dx, Inc. autoLDL | Medtest DX | 1 |
| Pointe Scientific, Inc. autoLDL Cholesterol | Horiba Instruments Incorporated | 1 |
Showing 12 of 26. All products under System, Test, Low Density, Lipoprotein
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K241800 | 2024-07-26 |
Recalls
2 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2023-01-27 | Class II | Under Investigation by firm | Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP), Triglycerides (Trig), and Triglycerides_2 (Trig_2) Impacting Magnesium (Mg) Results | 8420 units | |
| 2016-03-17 | Class II | Device Design | Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC) and Metamizole (Dipyrone) interference with Trinder and Trinder-like reaction assays. Siemens has confirmed that falsely depressed results may occur on samples drawn | 137422 units total | 2017-09-25 |
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.