International safety notice
Technical name: Instrumental Kit
Brazil / Anvisa · BRA · Dec 8, 2016
Key facts
| Title | Technical name: Instrumental Kit |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Instrumental Reflection Technical name: Instrumental Kit ANVISA registration number: 80804050103 Risk class: I Affected model: 71362106 - Reflection Guide Affected serial numbers: 15FM16705 / 15JM05524 / 15JM15006 / 15DM20374 / 15JM05522 / 15JM14 855 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO SMITH NEPHEW COMÉRCIO DE PRODUTOS MÉDICOS LTDA CNPJ 13656820000188 ENDEREÇO AVENIDA PRESIDENTE TANCREDO NEVES 272 JARDIM FLORESTA VARGEM GRANDE PAULISTASP BRASIL TELEFONES DE CONTATO 11 50709100 31972702 EMAIL DE CONTATO SACBRASILSMITHNEPHEWCOM FABRICANTE SMITH NEPHEW INC ORTHOPAEDIC DIVISION ENDEREÇO 1450 BROOKS ROAD MEMPHIS PAÍS ESTADOS UNIDOS DA AMÉRICA |
| Models | 80804050103, 71362106, 15FM16705, 15JM14855, 15DM20374, 15JM15006, 15JM05524, 15JM05522 |
| Date | Dec 8, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 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