International safety notice
Safety Notice for OPERA T, PRECISION RXi-T, MERATEL, BRT-20, CLINODIGIT COMPACT, FUTURA 2000 und ARKITON 90/20 M X-ray systems, GMM
Germany / BfArM · DEU · Jan 20, 2010
Key facts
| Title | Safety Notice for OPERA T, PRECISION RXi-T, MERATEL, BRT-20, CLINODIGIT COMPACT, FUTURA 2000 und ARKITON 90/20 M X-ray systems, GMM |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | OPERA T, PRECISION RXi-T, MERATEL, BRT-20, CLINODIGIT COMPACT, FUTURA 2000 und ARKITON 90/20 M X-ray systems, GMM |
| Manufacturer | Safety Notice for OPERA T, PRECISION RXi-T, MERATEL, BRT-20, CLINODIGIT COMPACT, FUTURA 2000 und ARKITON 90/20 M X-ray systems, GMM |
| Models | FSN01-09—ENG.DOC, 5117828, PAVIMENTO\FSN01_09_ENG.DOC, INCIDENTNCM01_09, 24068, 297787, 4525— |
| Date | Jan 20, 2010 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No 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