System, Measurement, Blood-pressure, Non-invasive
Philips North America Llc's record for this product code
MDR events34All time
Recalls0All time
510(k) clearances0All time
Recent MDR events
34 adverse event reports on file
- SURESIGNS VS2+ NBP/SPO2Sep 1, 2022Malfunction1218950-2022-00855
- SURESIGNS VSI - NBP/SPO2Aug 22, 2022Malfunction1218950-2022-00810
- SURESIGNS VSI - NBP/SPO2Aug 11, 2022Malfunction1218950-2022-00708
- SURESIGNS VSI - NBPJul 18, 2022Malfunction1218950-2022-00606
- SURESIGNS VS2+ NBP/SPO2Jun 29, 2022Malfunction1218950-2022-00526
- SURESIGNS VS2+ NBP/SPO2Jun 15, 2022Malfunction1218950-2022-00499
- SURESIGNS VS4 NBP, SPO2Jun 14, 2022Malfunction1218950-2022-00492
- SURESIGNS VS2+ NBP/SPO2Apr 8, 2022Malfunction1218950-2022-00318
- SURESIGNS VS2+ NBP/SPO2Apr 4, 2022Malfunction1218950-2022-00298
- SURESIGNS VSI - NBP/SPO2Mar 29, 2022Malfunction1218950-2022-00271
Recalls
0 recall events for this product code
No recalls on file for Philips North America Llc under this product code.
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for Philips North America Llc under this product code.