International safety notice
Commercial name: Endokit/// Registration Number: 80689090090 /// Risk Class: III (High Risk)/// Affected models: REK24N / REK26N/// Affected batches: NGYIX401;
Brazil / Anvisa · BRA · Sep 12, 2016
Key facts
| Title | Commercial name: Endokit/// Registration Number: 80689090090 /// Risk Class: III (High Risk)/// Affected models: REK24N / REK26N/// Affected batches: NGYIX401 ; |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Endokit/// Registration Number: 80689090090 /// Risk Class: III (High Risk)/// Affected models: REK24N / REK26N/// Affected batches: NGYIX401 ; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO BARD BRASIL INDÚSTRIA E COMÉRCIO DE PRODUTOS MEDICOS LTDA FABRICANTE |
| Models | NGYIX401, REK26N, NGYIX402, 80689090090, REK24N, NGZG1732 |
| Date | Sep 12, 2016 |
| 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