International safety notice
Technical name: Instrumental Kit
Brazil / Anvisa · BRA · Oct 9, 2017
Key facts
| Title | Technical name: Instrumental Kit |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Zimmer Biomet Drills - Trauma Technical name: Instrumental Kit ANVISA registration number: 80245480015; Risk class: I Affected model: 4806-110-35; Affected serial numbers: 480611035 63364063; 249007543 63413801; 480723025 63431786; 236017520 63481881 236015327 63524034; 236020527 63557936; 480611035 63431723 480610020 63451655; 480610027 63462196 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO WM WORLD MEDICAL IMP EXP LTDA CNPJ 03179994000143 RUA DO REZENDE 189 RIO DE JANEIRO RJ FABRICANTE ZIMMER INC WARSAW ESTADOS UNIDOS |
| Models | 63524034, 480611035, 4807-230-25, 80245480015, 249007543, 63431786, 2360-153-27, 2490-75-43, 236015327, 80245480052, 63481881, 2360-175-20 and 16 more |
| Date | Oct 9, 2017 |
| 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