International safety notice
Catheters
Brazil / Anvisa · BRA · Jul 19, 2017
Key facts
| Title | Catheters |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Turbo Elite Technical name: Catheters ANVISA registration number: 80628940030 Risk class: III Affected model: 414-159/420-159 Affected serial numbers: Mod:: 414-159 - FBF16G07A (5) and FBF16L15D (5) /Mod: 420-159 - FBH16G18A (7), FBH16L17A(5) and FBH16L16B (2) |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO MN MEDICA REP E COM EQ MÉDICOS ESTÉTICOS E COSMÉTICOS LTDA CNPJ 10845671000107 RUA BORGES LAGOA 1065 CJ 63 SÃO PAULO SP FABRICANTE MN MEDICA REP E COM EQ MÉDICOS ESTÉTICOS E COSMÉTICOS 9965 FEDERAL DRIVE COLORADO SPRINGS 80921 ESTADOS UNIDOS DA AMÉRICA TELEFONE 1 800800 2310978 EMAIL CUSTOMERSERVICESPNCCOM |
| Models | FBH16L16B, FBF16L15D, FBF16G07A, FBH16G18A, FBH16L17A, 420-159, 414-159, 80628940030 |
| Date | Jul 19, 2017 |
| 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