International safety notice
Technical name: Vascular Catheter Introduction Kit, Steerable
Brazil / Anvisa · BRA · Mar 20, 2017
Key facts
| Title | Technical name: Vascular Catheter Introduction Kit, Steerable |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Where to use the mobile device. Technical name: Kit for Vascular Category Introduction, Registrar Registration Number ANVISA: 80145901385 Rescue Class: IV Model afetado: Mobicath Curva Curta and Curva Long Number of Series afetados: SKU D140010, lots: W3332609 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO JOHNSON JOHNSON DO BRASIL IND E COM DE PROD PARA SAÚDE LTDA CNPJ 54516661000101 LOCALIZADA NA AV JUSCELINO KUBITSCHEK Nº 2041 ANDARES 8º E 9º COMPLEXO JK BLOCO B SÃO PAULO SP FABRICANTE GREATBATCH MEDICAL 2300 BERKSHIRE LANE NORTH PLYMOUTH MINNEAPOLIS MN 55441 |
| Models | W3501354, W3441735, W3374699, X3586059, X3537038, W3501348, W3384701, W3357184, W3507597, W3479706, W3494912, X3497121 and 86 more |
| Date | Mar 20, 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