International safety notice
Commercial name: Sinus SuperFlex 635 Technical Name: Stent Registration: 80134860182 Model: Length 200 mm Lots Q010281;
Brazil / Anvisa · BRA · Aug 20, 2015
Key facts
| Title | Commercial name: Sinus SuperFlex 635 Technical Name: Stent Registration: 80134860182 Model: Length 200 mm Lots Q010281; |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Sinus SuperFlex 635 - Registration 80134860182 Risk Class III (High Risk) Model: Length 200 mm Lots Q010281; |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL GRIFOLS BRASIL LTDA CNPJ 02513899000171 ENDEREÇO RUA UMUARAMA N 263 PINHAIS PR TELEFONE 41 36682444 FABRICANTE OPTIMED MEDIZINISCHE INSTRUMENTE GMBH FERDINANDPORSCHESTRASSE ALEMANHA |
| Models | Q018124, sinus-SuperFlex-635, Q011544, Q016211, Q012989, Q010281, Q011147, Q012048, Q016213, Q014025, 80134860182, Q020471 and 7 more |
| Date | Aug 20, 2015 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
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