International safety notice
Weight restrictions for Bicontact SD and Bicontact SD-Revision implants from Aesculap
Germany / BfArM · DEU · Jan 10, 2005
Key facts
| Title | Weight restrictions for Bicontact SD and Bicontact SD-Revision implants from Aesculap |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Bicontact SD and Bicontact SD-Revision implants from Aesculap |
| Manufacturer | Weight restrictions for Bicontact SD and Bicontact SD-Revision implants from Aesculap |
| Models | 95-2600, ACCORDIN9, NK709T, 00028, NJ20BT, D-78532, NJ208T, 93142, 21060, N3209T, NK210T, 931421EWG and 11 more |
| Date | Jan 10, 2005 |
| 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