International safety notice
Urgent Field Safety Notice for FLEX Monoclonal Rabbit Anti-Human Estrogen Receptor by Agilent Technologies Denmark ApS
Germany / BfArM · DEU · Aug 13, 2019
Key facts
| Title | Urgent Field Safety Notice for FLEX Monoclonal Rabbit Anti-Human Estrogen Receptor by Agilent Technologies Denmark ApS |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | FLEX Monoclonal Rabbit Anti-Human Estrogen Receptor |
| Manufacturer | Agilent Technologies Denmark ApS |
| Models | M364301, «ADDRESS2», CAPA00722, IR657, IS084, 10125849, IS657, GA084, 10127400, IR084, «ADDRESS1», 10127880 and 1 more |
| Date | Aug 13, 2019 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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