Rapidpoint® 340 Sensor Module
RAPIDPOINT® 340 Sensor Module, an in vitro diagnostics device to be used on the RAPIDPOINT® 340 analyzer
1manufacturer
1catalogue number
Who Else Makes It
Registered in Guangdong.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Edan Instruments, Inc. | Shenzhen | Guangdong | Contract manufacturer | 56 |
Record
| Listed by | Siemens Healthcare Diagnostics Inc, United States |
|---|---|
| FDA product code | JFP |
| Device type | Electrode, Ion Specific, Calcium |
| Device class | Class 2 |
| Regulation | 21 CFR 862.1145 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| 510(k) | K021515 |
| Record published | 2016-09-24 |
| Record revised | 2021-11-19 (version 5) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Storage | Storage environment temperature 5 to 25 °C |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 10375809 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Stat Profile | Nova Biomedical Corporation | 9 |
| Nova | Nova Biomedical Corporation | 8 |
| Calcium Electrode | Medica Corp. | 2 |
| SC90 | Radiometer Medical APS | 2 |
| pH/pCO2/pO2/Na/K/Ca Analyzer | Medica Corp. | 2 |
| Na/K/Cl/Ca/Li Solution pack | Medica Corp. | 1 |
| Rinse Solution S4980 REF 944-130 | Radiometer Medical APS | 1 |
| Nova/Stat Profile | Nova Biomedical Corporation | 1 |
| Rapidpoint® 350 Sampler Module | Siemens Healthcare Diagnostics Inc | 1 |
| RAPIDLab® 1200 pH Electrode Fill | Siemens Healthcare Diagnostics Inc | 1 |
| Roche 9180 Electrolyte Analyzer | Roche Diagnostics Gmbh | 1 |
| E-Ca Cassette Carton | Opti Medical Systems Inc. | 1 |
Showing 12 of 33. All products under Electrode, Ion Specific, Calcium
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 |
|---|---|---|---|---|---|---|
| Medica Corp. | 510(k) number | 2025-12-31 | Class II | Nonconforming Material/Component | A systematic positive bias of up to 20% was identified across the reportable potassium range, resulting in false elevation results of patient samples when using Medica s capillary tubes. | 1,578 units |
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.