International safety notice
Technical Name: Bone Graft - Risk Class IV - Maximum Risk
Brazil / Anvisa · BRA · Sep 23, 2013
Key facts
| Title | Technical Name: Bone Graft - Risk Class IV - Maximum Risk |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Jectos injectable synthetic bone substitute - Registration No. 80240590014 - Model: J406C05 - Lot: 406/13204 |
| Manufacturer | IMPORTADOR ORTECH MEDICAL COMÉRCIO IMPORTAÇÃO E EXPORTAÇÃO LTDA CNPJ 06328384000152 RUA JORGE AUGUSTO 83 SALAS 55 A 58 SÃO PAULOSP TELEFONE 11 25323710 |
| Models | 13204, 80240590014, J406C05 |
| Date | Sep 23, 2013 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 100–999 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