International safety notice
Urgent field safety notice for BladderScan® BVI 9600 und AortaScan® AMI 9700, Verathon Inc.
Germany / BfArM · DEU · Jun 14, 2016
Key facts
| Title | Urgent field safety notice for BladderScan® BVI 9600 und AortaScan® AMI 9700, Verathon Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | BladderScan® BVI 9600 und AortaScan® AMI 9700, Verathon Inc. |
| Manufacturer | Urgent field safety notice for BladderScan® BVI 9600 und AortaScan® AMI 9700, Verathon Inc. |
| Models | 20RECALL, 0270-0452, 31.30.68.70.512, 800.331.2313, A7000000, 20SAF, 20SAFETY, 20RECALLMAILTO, 20AND, ©2015, 98011, 20REUSABLE and 10 more |
| Date | Jun 14, 2016 |
| Regulator page | bfarm.de |
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