International safety notice
Kit Instrumental
Brazil / Anvisa · BRA · Sep 10, 2015
Key facts
| Title | Kit Instrumental |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | ZIMMER GUIDE WIRE, Models 2228-24, 47-2237-33 - Registration - 80245480007 - Lots 60996288, 61030793, 61020362, 61030778, 61020362; |
| Manufacturer | DETENTOR DO REGISTRO WM WORLD MEDICAL IMP EXP LTDA CNPJ 03179994000143 ENDEREÇO RUA DO REZENDE RIO DE JANEIRO RJ FABRICANTE ZIMMER INC ESTADOS UNIDOS |
| Models | 61030778, 2255-25, 61745826, 61723543, 61291089, 80245480007, 2228-24, 2255-26, 61020362, 60701262, 80245480015, 47-2237-33 and 3 more |
| Date | Sep 10, 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