International safety notice
Technical Name: INSTRUMENTAL KIT
Brazil / Anvisa · BRA · Jul 1, 2016
Key facts
| Title | Technical Name: INSTRUMENTAL KIT |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial Name: MIS INSTRUMENTAL FOR KNEE ARTHROPLASTY////////registration 80005430186 ////Serial lot: SB8H28T; |
| Manufacturer | DADOS DO DETENTOR DO REGISTRO NO BRASIL STRYKER DO BRASIL LTDA RUA URUSSUÍ 300 7 ANDAR SÃO PAULO SP CEP 05022001 CNPJ 01716863000101 FONE 11 51892503 OU 28927469 EMAIL QUALIDADESTRYKERCOM FABRICANTES STRYKER LEIBINGER GMBH COALEMANHA HOWMEDICA OSTEONICS CORP ESTADOS UNIDOS DA AMÉRICA |
| Models | SB8S43X, SB8S43A, SB8V41, SB8S43P, SB9C23, SB8V41J, SB8H28T, 80005430186, SB8V41K |
| Date | Jul 1, 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