International safety notice
Angiography Equipment
Brazil / Anvisa · BRA · Mar 29, 2017
Key facts
| Title | 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 Affected model: Allura Xper FD10 Ceiling/ Allura Xper FD10 Floor/ Allura FD10 OR Table/ Allura 1751, 538; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO PHILIPS MEDICAL SYSTEMS LTDA CNPJ 58295213000178 ENDEREÇO AV TAMBORÉ 14001440 BOX 31 A 33 TAMBORÉ BARUERISP BRASIL CEP 06460000 TELEFONE PARA SUPORTE 08007017789 FABRICANTE PHILIPS MEDICAL SYSTEMS NEDERLAND BV DIXTAL BIOMÉDICA INDÚSTRIA E COMÉRCIO LTDA PHILIPS MEDICAL SYSTEMS LTDA ENDEREÇOS VEENPLUIS 46 5684 PC BEST HOLANDA AV RODRIGO OTÁVIO 1111 MANAUS AM CEP 69077000 BRASIL RUA PREFEITO ELIZEU ALVES DA SILVA 400 CEP 33400000 LAGOA SANTA MINAS GERAIS BRASIL |
| Models | 10216710153, 00051432 |
| Date | Mar 29, 2017 |
| 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