International safety notice
Technical name: 2501190 - Catheters
Brazil / Anvisa · BRA · Dec 18, 2017
Key facts
| Title | Technical name: 2501190 - Catheters |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Softip Guider Guide Catheter Technical name: 2501190 - Catheters ANVISA registration number: 80005430399 Risk class: IV Affected model: SEE ANNEX I Affected serial numbers: SEE ANNEX I |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO STRYKER DO BRASIL LTDA CNPJ 02966317000102 RUA URUSSUÍ 300 SÃO PAULO SP FABRICANTE BOSTON SCIENTIFIC CORPORATION 300 BOSTON SCIENTIFIC WAY MARLBOROUGH MA 01752 ESTADOS UNIDOS |
| Models | 2501190, 80005430399 |
| Date | Dec 18, 2017 |
| 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