International safety notice
Angiography Equipment
Brazil / Anvisa · BRA · Nov 9, 2015
Key facts
| Title | Angiography Equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | ALLURA XPER ANGIOGRAPHY EQUIPMENT, brand PHILIPS, Risk class: III, model: ALLURA |
| Manufacturer | DETENTOR DO REGISTRO PHILIPS MEDICAL SYSTEMS LTDA CNPJ 58295213000178 ENDEREÇO AV PIRACEMA 1411 MÓDULOS 3 E 4 TAMBORÉ BARUERI SP FABRICANTE PHILIPS MEDICAL SYSTEMS NEDERLAND BV ENDEREÇO VEENPLUIS 46 5684 PC BEST HOLANDA |
| Models | 10216710206, 10216710153 |
| Date | Nov 9, 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