International safety notice
Device for implanting intraocular lenses
Brazil / Anvisa · BRA · Dec 20, 2013
Key facts
| Title | Device for implanting intraocular lenses |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Disposable Injector for Implantation of OFT VISION Foldable Intraocular Lens, Injector Model 2.8 Registration nº 80153650024, batch: IN280070911 |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL OFT VISION INDÚSTRIA E COMÉRCIO LTDA CNPJ 74215014000114 ENDEREÇO RUA IMBOCUÍ 279283 SÃO PAULO SÃO PAULO TELEFONE 11 20927023 |
| Models | IN280070911, 80153650024 |
| Date | Dec 20, 2013 |
| 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