International safety notice
VIDEOBRONCOSCOPIO EVIS EXERA II OLYMPUS BF TIPO 1T180 (BF-1T180); VIDEOBRONCOSCOPIO EVIS EXERA OLYMPUS BF TIPO XT160 (BF- XT160)
Spain / AEMPS · ESP · Sep 24, 2020
Key facts
| Title | VIDEOBRONCOSCOPIO EVIS EXERA II OLYMPUS BF TIPO 1T180 (BF-1T180); VIDEOBRONCOSCOPIO EVIS EXERA OLYMPUS BF TIPO XT160 (BF- XT160) |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | VIDEOBRONCOSCOPIO EVIS EXERA II OLYMPUS BF TIPO 1T180 (BF-1T180); VIDEOBRONCOSCOPIO EVIS EXERA OLYMPUS BF TIPO XT160 (BF- XT160) |
| Manufacturer | Olympus Medical Systems Corporation, Japón. |
| Models | 2020-554, BF-XT160, “BF-1T180, 28022, 29-31, 153-011, 08908, 91.822.52.89, 62174, 05.10.2020, XT160, “BF-160” and 8 more |
| Event type | Safety Notice |
| Date | Sep 24, 2020 |
At a glance
- No Recall
- Yes 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