International safety notice
GRANVIA-C, IMPIX ALIF, IMPIX C+, IMPIX MANTA, IMPIX S, PASS LP, IMPIX 3D, IMPIX ALIF S/A, IMPIX DLIF, IMPIX MANTA+, IMPIX TLIF. Ver referencias afectadas en España en el Anexo A de la nota de aviso de la empresa
Spain / AEMPS · ESP · Jul 24, 2023
Key facts
| Title | GRANVIA-C, IMPIX ALIF, IMPIX C+, IMPIX MANTA, IMPIX S, PASS LP, IMPIX 3D, IMPIX ALIF S/A, IMPIX DLIF, IMPIX MANTA+, IMPIX TLIF. Ver referencias afectadas en España en el Anexo A de la nota de aviso de la empresa |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | GRANVIA-C, IMPIX ALIF, IMPIX C+, IMPIX MANTA, IMPIX S, PASS LP, IMPIX 3D, IMPIX ALIF S/A, IMPIX DLIF, IMPIX MANTA+, IMPIX TLIF. Ver referencias afectadas en España en el Anexo A de la nota de aviso de la empresa |
| Manufacturer | Medicrea International S.A., Francia. |
| Models | 19D0071, 28050, 17-MAR-2023, 19L0032, B13111036, 21D0097, 20F0921, 19J0465, B15130611S, B13111025, 19B0395, A13131516 and 68 more |
| Event type | Safety Notice |
| Date | Jul 24, 2023 |
At a glance
- No Recall
- Yes 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