International safety notice
Technical name: Guide for Introducing Catheters
Brazil / Anvisa · BRA · Jun 19, 2017
Key facts
| Title | Technical name: Guide for Introducing Catheters |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: NITINOL GUIDE FOR URODRAIN PROMEDON CATHETER Technical name: Guide for Catheter Introduction ANVISA registration number: 10306840122 Risk class: II Affected model: G-35-150S-NIT Affected serial numbers: Code: G-35- 150S-NIT Lots: 30892 to 30901; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO PROMEDON DO BRASIL PRODUTOS MEDICO HOSPITALARES AV GUIDO CALOI 1935 BL C1 SÃO PAULO SP 11 35956741 FABRICANTE PROMEDON SA AV GRAL MANUEL SAVIO SN LOTE 3 MANZANA 3 CÓRDOBA ARGENTINA 0351 4502100 |
| Models | 32306, 32139, 30901, G-35-150S-NIT, 31442, 31484, 31907, 32680, 10306840122, 31113, 31430, 31777 and 13 more |
| Date | Jun 19, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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