International safety notice
Technical name: CENTRIFUGAL PUMP FOR CARDIOPULMONARY BY-PASS SYSTEM
Brazil / Anvisa · BRA · May 15, 2017
Key facts
| Title | Technical name: CENTRIFUGAL PUMP FOR CARDIOPULMONARY BY-PASS SYSTEM |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: PERFUSION SYSTEM Technical name: CENTRIFUGAL PUMP FOR CARDIOPULMONARY BY-PASS SYSTEM ANVISA registration number: 80102511251 Risk class: III Affected model: S5, C5 Affected serial numbers: NS 16S15049 and 16S15050 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODS MÉDICOS LTDA CNPJ04718143000194 ENDEREÇO RUA BATATAES 391 CONJS 1112 E 13 MUNICÍPIO SÃO PAULO UF SP FABRICANTE LIVANOVA DEUSTCHLAND GMBH ANTIGA SORIN DEUSTCHLAND GMBH ENDEREÇO LINDBERGHSTRASSE 25 MUNIQUE ALEMANHA |
| Models | 16S15049, 80102511251, 16S15050 |
| Date | May 15, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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