International safety notice
Technical name: Angiography Equipment
Brazil / Anvisa · BRA · Sep 23, 2016
Key facts
| Title | Technical name: Angiography Equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Allura Xper Angiography Equipment Technical name: Angiography Equipment ANVISA registration number: 10216710153 Risk class: III - High Risk Affected models: ALLURA XPER FD10 OR table; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO PHILIPS MEDICAL SYSTEMS LTDA CNPJ 58295213000178 AV TAMBORÉ 14001440 BOX 31 A 33 TAMBORÉ BARUERISP TELEFONE 11 97576360811 21250023 FABRICANTE PHILIPS MEDICAL SYSTEMS NEDERLAND BV VEENPLUIS 46 5684 PC BEST HOLANDA |
| Models | 10216710153 |
| Date | Sep 23, 2016 |
| 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