International safety notice
Kit Instrumental
Brazil / Anvisa · BRA · Feb 5, 2016
Key facts
| Title | Kit Instrumental |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | INSTRUMENTAL FOR TS STRYKER TRAUMA RODS, Guide Wire, registration 80005430088, risk class I, lots/series: K076CCF; |
| Manufacturer | DETENTOR DO REGISTRO STRYKER DO BRASIL LTDA CNPJ 02966317000102 ENDEREÇO RUA URUSSUÍ 300 7 ANDAR SÃO PAULOSP FABRICANTE STRYKER TRAUMA GMBH END PROF KUENTSCHER STRASSE 15D 24232 SCHOENKIRCHENKIEL |
| Models | K0AF3C9, K261793, K07B727, K07EF49, K043C6B, K0B8538, K076CCF, K282163, K487845, 80005430088, K083C1D, K785079 and 5 more |
| Date | Feb 5, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 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