International safety notice
Corrective action for the products VIVA II, PRISMA II and MELODY II (Sleep apnea devices), anamed GmbH & Co. KG
Germany / BfArM · DEU · Jun 23, 2015
Key facts
| Title | Corrective action for the products VIVA II, PRISMA II and MELODY II (Sleep apnea devices), anamed GmbH & Co. KG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the products VIVA II, PRISMA II and MELODY II (Sleep apnea devices), anamed GmbH & Co. KG |
| Manufacturer | Corrective action for the products VIVA II, PRISMA II and MELODY II (Sleep apnea devices), anamed GmbH & Co. KG |
| Models | 31100015, 2015-06-09, D-56130, 56130 |
| Date | Jun 23, 2015 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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