International safety notice
Bone Graft - rectification
Brazil / Anvisa · BRA · Sep 21, 2015
Key facts
| Title | Bone Graft - rectification |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Actifuse ABX 1-2mm, manufacturer Apatech, models 506005078047 (2.5mm); |
| Manufacturer | DETENTORA DO REGISTRO OSTEOCAMP IMPLANTES E MATERIAIS CIRÚRGICOS LTDA CNPJ 04556194000167 ENDEREÇO AV CAMBACICA KM 1145 Nº 1200 COND FLEX BUILDINGS MODULO 7 ANHUMAS CAMPINAS SP FABRICANTE APATECH LIMITED ENDEREÇO 370 CENTENNIAL PARK WD6 3TJ ELSTREE REINO UNIDO |
| Models | 506005078048, 506005078047, 506005078049, 80253610018 |
| Date | Sep 21, 2015 |
| Regulator page | anvisa.gov.br |
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