International safety notice
Technical Name: Surgical instruments
Brazil / Anvisa · BRA · May 10, 2016
Key facts
| Title | Technical Name: Surgical instruments |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial Name: Aprima Percutaneous Access Set - Reg.10212990312 - Class II-medium risk; |
| Manufacturer | DETENTORA DO REGISTRO NO BRASIL E TAMUSSINO CIA LTDA 33100082000103 RUA WASHINGTON LUÍS 97 E 95 LOJA B RIO DE JANEIRO RJ 21 32218570 FABRICANTE COOK INCORPORATED ESTADOS UNIDOS DANIELS WAY BLOOMINGTON IN 47404 TELEFONE 800 457 4500 |
| Models | Reg.10212990312, 5146406, NPAS-104-HC-NT-U-SST, NS5469905, NS5469904, 5146407 |
| Date | May 10, 2016 |
| 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