International safety notice
Alert 2547 (Technosurveillance) - Philips - Allura Xper Angiography Equipment System may freeze after a certain period of continuous operation.
Brazil / Anvisa · BRA · Apr 17, 2018
Key facts
| Title | Alert 2547 (Technosurveillance) - Philips - Allura Xper Angiography Equipment System may freeze after a certain period of continuous operation. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Allura Xper Angiography Equipment Technical name: Angiography Equipment ANVISA registration number: 10216710153 Risk class: III Model affected: Allura Xper FD10 Ceiling/ Allura Xper FD10 Floor/ Allura Xper FD20 Ceiling/ Allura Xper FD20 Floor/ Allura Xper FD10 OR Table/ Allura Xper FD20 or Table Affected serial numbers: 947 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO PHILIPS MEDICAL SYSTEMS LTDA CNPJ 58295213000178 AV TAMBORÉ 14001440 BOX 31 A 33 TAMBORÉ BARUERI SÃO PAULO TEL 11 975763608 21250023 EMAIL LARISSAFRIASPHILIPSCOM FABRICANTE PHILIPS MEDICAL SYSTEMS NEDERLAND B V VEENPLUIS 46 5584 PC BEST HOLANDA EMAIL REGULATORIOSPHILIPSCOM |
| Models | 10216710153 |
| Date | Apr 17, 2018 |
| 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