International safety notice
Safety Notice: Update of the instructions for use of the ELEVATE Apical and Posterior Prolapse Repair System, AMS
Germany / BfArM · DEU · Nov 22, 2011
Key facts
| Title | Safety Notice: Update of the instructions for use of the ELEVATE Apical and Posterior Prolapse Repair System, AMS |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | use of the ELEVATE Apical and Posterior Prolapse Repair System, AMS |
| Manufacturer | Safety Notice: Update of the instructions for use of the ELEVATE Apical and Posterior Prolapse Repair System, AMS |
| Models | CONSUMER.AFFAIRS2, 00621, 55343, 10700, 952-930-6157, 952-930-6000 |
| Date | Nov 22, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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