International safety notice
Exoplan. Cuando se utiliza un método de tratamiento quirúrgico totalmente guiado con CAMLOG® Screw-Line Promote® implantes guiados/atornillados con CAMLOG® Screw-Line Guide System o anillas StecoGuide para el sistema Screw-Line.
Spain / AEMPS · ESP · Nov 20, 2023
Key facts
| Title | Exoplan. Cuando se utiliza un método de tratamiento quirúrgico totalmente guiado con CAMLOG® Screw-Line Promote® implantes guiados/atornillados con CAMLOG® Screw-Line Guide System o anillas StecoGuide para el sistema Screw-Line. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Exoplan. Cuando se utiliza un método de tratamiento quirúrgico totalmente guiado con CAMLOG® Screw-Line Promote® implantes guiados/atornillados con CAMLOG® Screw-Line Guide System o anillas StecoGuide para el sistema Screw-Line. |
| Manufacturer | Exocad GmbH, Alemania. |
| Models | 39110, K1045.3311, 14013, K1045.4316, 74321, K1045.3816, 99414, 91.822.52.89, J37X4.3303, J37X4.4303, 278955, M.27.15.D450L3 and 47 more |
| Event type | Safety Notice |
| Date | Nov 20, 2023 |
At a glance
- No Recall
- Yes 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