Catalogue number 11170852, listed by Siemens Healthcare Diagnostics Inc, United States, under Calibrator For Hemoglobin And Hematocrit Measurement. 2 manufacturers in China are registered for this product code.
Who Else Makes It
Concentrated in Jilin (1), Guangdong (1).
Record
Regulatory record for Advia® 360/560 Calibrator | Listed by | Siemens Healthcare Diagnostics Inc, United States |
| FDA product code | KRZ |
| Device type | Calibrator For Hemoglobin And Hematocrit Measurement |
| Device class | Class 2 |
| Regulation | 21 CFR 864.8165 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| 510(k) | K955925 |
| Record published | 2016-09-24 |
| Record revised | 2021-11-18 (version 5) |
Specifications
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 |
Recalls
1 of these is 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.
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.