International safety notice
IDKmonitor® Infliximab total ADA. K 9654. IDKmonitor® Adalimumab total ADA. K 9651. Remsima® Monitor total ADA. K 9664. 25(OH)-Vitamin D direct day ELISA. K 2108. 25(OH)-Vitamin D dried blood ELISA. K 2108DBS. PreventID® Cardiac Troponin I. KSTCTI402
Spain / AEMPS · ESP · Jul 23, 2019
Key facts
| Title | IDKmonitor® Infliximab total ADA. K 9654. IDKmonitor® Adalimumab total ADA. K 9651. Remsima® Monitor total ADA. K 9664. 25(OH)-Vitamin D direct day ELISA. K 2108. 25(OH)-Vitamin D dried blood ELISA. K 2108DBS. PreventID® Cardiac Troponin I. KSTCTI402 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | IDKmonitor® Infliximab total ADA. K 9654. IDKmonitor® Adalimumab total ADA. K 9651. Remsima® Monitor total ADA. K 9664. 25(OH)-Vitamin D direct day ELISA. K 2108. 25(OH)-Vitamin D dried blood ELISA. K 2108DBS. PreventID® Cardiac Troponin I. KSTCTI402 |
| Manufacturer | Immundiagnostik AG, Alemania |
| Models | 64625, 9651.REMSIMA®, 849430, KSTCTI402.PREVENTID®, 2108DBS, HYVEDEMM479, 91.822.52.89, 2019-391, 1329474, 2108.25, 24077, 601308630 and 13 more |
| Event type | Safety Notice |
| Date | Jul 23, 2019 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1