International safety notice
Technical name: Bone Distractor
Brazil / Anvisa · BRA · Oct 6, 2016
Key facts
| Title | Technical name: Bone Distractor |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Maxillofacial Distraction System Technical name: Bone Distractor ANVISA registration number: 80145901599 Risk class: III Affected model: Distr. |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO JOHNSON JOHNSON DO BRASIL IND E COM DE PROD PARA SAÚDE LTDA CNPJ 54516661000101 LOCALIZADA NA AV JUSCELINO KUBITSCHEK Nº 2041 ANDARES 8º E 9º COMPLEXO JK BLOCO B SÃO PAULO SP FABRICANTE SYNTHES GMBH LOCALIZADA NO ENDEREÇO EIMATTSTRASSE 3 CH 4436 OBERDORF SUÍÇA |
| Models | 5859710, 487.974, 487.965, 487.964, 5868674, 7865438, 487.963, 5354033, 6107609, 5860826, 7537258, 487.975 and 7 more |
| Date | Oct 6, 2016 |
| 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