International safety notice
Technical name: Angiography Equipment
Brazil / Anvisa · BRA · Jan 10, 2017
Key facts
| Title | Technical name: Angiography Equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Allura Xper Angiography Equipment Brand Philips Technical name: Angiography Equipment ANVISA registration number: 10216710153 Risk class: III Shaped model: Allura Xper FD10 Teto/ Allura Xper FD10 Chão/ Allura Xper FD20 Teto/ Allura Affected serial numbers: 285; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO PHILIPS MEDICAL SYSTEMS LTDA CNPJ 58295213000178 AV TAMBORÉ 14001440 BOX 31 A 33 TAMBORÉ BARUERI SP FABRICANTE PHILIPS MEDICAL SYSTEMS NEDERLAND BV VEENPLUIS 46 5684 PC BEST HOLANDA EMAIL REGULATORIOSPHILIPSCOM |
| Models | 10216710153 |
| Date | Jan 10, 2017 |
| 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