International safety notice
Angiography Equipment
Brazil / Anvisa · BRA · Mar 20, 2015
Key facts
| Title | Angiography Equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | SISTEMA DE ANGIOGRAFIA INTEGRIS ALLURA, ALLURA XPER, Modelo: H5000F/Allura Xper FD10 Teto/ Allura Xper FD10 Chão/ Allura Xper FD20 Teto/ Allura Xper FD20 Chão/ Allura Xper FD10 OR Table/ Allura Xper FD20 OR Table / Allura Xper FD10/10; Allura Xper FD20/10; Allura Xper FD20/20; Allura Xper FD10/10 OR Table; Allura Xper FD20/10 OR Table; Allura Xper FD20/20 OR Table/ Integris Allura 12/15 Integris Allura 12/15F Integris Allura 9C Integris Allura 9F Affected records: 10216710034/// 10216710153/// 10216710155/// 10216710206. Affected serial numbers: 176 / 553 / 759 / 1751 / 001H021796 / 001H021878 / S4F010159A / S4F200174A / S4F200270A. |
| Manufacturer | DETENTOR DO REGISTRO PHILIPS MEDICAL SYSTEMS LTDA CNPJ AV PIRACEMA 1411 MÓDULOS 3 E 4 TAMBORÉ BARUERI SÃO PAULO FABRICANTE PHILIPS MEDICAL SYSTEMS CLEVELAND INC 595 MINER ROAD CLEVELAND OH 44143 EUA |
| Models | 001H021878, 10216710206, S4F200270A, H5000F, 10216710034, 10216710153, S4F010159A, S4F200174A, 10216710155, 001H021796 |
| Date | Mar 20, 2015 |
| 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