International safety notice
Cepheld Xpert Xpress Strep A - pipetid ei pruugi väljastada piisavat proovikogust
Estonia / EMDDB · EST · Nov 1, 2023
Key facts
| Title | Cepheld Xpert Xpress Strep A - pipetid ei pruugi väljastada piisavat proovikogust |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Cepheld Xpert Xpress Strep A |
| Manufacturer | CEPHELD XPERT XPRESS STREP |
| Models | 25-Feb-24, 17-Mar-24, 23815, 18-Feb-24, 1000535892, 03-Sep-23, 1000495394, 1000501407, 1000494468, 1000522877, 23608, 1000489420 and 161 more |
| Date | Nov 1, 2023 |
| Regulator page | terviseamet.ee |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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