International safety notice
Angiography equipment
Brazil / Anvisa · BRA · Feb 5, 2015
Key facts
| Title | Angiography equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Angiography equipment, Risk class: III, models described below: Model: ALLURA XPER FD10 (floor), ALLURA XPER FD10 (ceiling), ALLURA XPER FD20 (floor), ALLURA Modelo: INTEGRISH5000 F, Registro:10216710034 //// Modelo: Integris Allura 12/15, Integris Allura 12/15F, Integris Allura 9C, Integris Allura 9F; Modelo: 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; Registro: 10216710206. Serial number: 176 ; |
| Manufacturer | DETENTOR DO REGISTRO PHILIPS MEDICAL SYSTEMS LTDA CNPJ 58295213000178 ENDERÇO AV PIRACEMA 1411 MÓDULOS 3 E 4 TAMBORÉ BARUERI SP FABRICANTE PHILIPS MEDICAL SYSTEMS NEDERLAND BV ENDERÇO VEENPLUIS 46 5684 PC BEST HOLANDA |
| Models | 10216710153, 10216710206, S4F200270A, S4F200174A, S4F010159A, 001H021796, 10216710034, INTEGRISH5000, 10216710155, 001H021878 |
| Date | Feb 5, 2015 |
| 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