International safety notice
Technical name: Stryker Cementless Hip System
Brazil / Anvisa · BRA · Oct 3, 2016
Key facts
| Title | Technical name: Stryker Cementless Hip System |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: PROT Q HEAD V40 LFIT 36MM/5 /// Technical name: Stryker Uncemented Hip System /// ANVISA registration number: 80005430152 /// Risk class: III - High Risk /// Affected serial numbers : See Distribution map |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO STRYKER DO BRASIL LTDA CNPJ 02966317000102 RUA URUSSUÍ 300 7 ANDAR ITAIM BIBI SÃO PAULOSP TELEFONE 11 51892503 EMAIL AMERICOFELIXSTRYKERCOM FABRICANTE STRYKER ORTHOPAEDICS 325 CORPORATE DRIVE MAHWAH NJ 07430 ESTADOS UNIDOS |
| Models | 80005430152 |
| Date | Oct 3, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 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