International safety notice
Technical Name: Angiography Equipment
Brazil / Anvisa · BRA · Jun 23, 2016
Key facts
| Title | Technical Name: Angiography Equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Allura Xper Angiography Equipment ANVISA registration number: 10216710153 Risk class: III Modelo(s) afetado(s): Allura Xper FD1O / Allura Xper FD1O/10 / Allura Xper FD2O / Allura Xper FD2O/10 biplane / Allura Xper FD1 0 OR Table / Allura Xper FD1O/10 OR Table / Allura Xper FD2O OR Table / Allure Xper FD2O/20 / Allura Xper FD2O/20 biplane OR Table / Allura Xper FD2O/1 5 / Allura Xper FD2O/1 5 OR Table List of batches/series: 285 / 306 / 308 / 322 / 379 / 565 / 405 / 639 |
| Manufacturer | DETENTOR DO REGISTRO DO PRODUTO NO BRASIL NOME PHILIPS MEDICAL SYSTEMS LTDA CNPJ 58295213000178 ENDEREÇO AV TAMBORÉ 14001440 BOX 31 A 33 TAMBORÉBARUERI UF SP TELEFONE DE CONTATO 11 96910904511 21250023 FABRICANTE PHILIPS MEDICAL SYSTEMS NEDERLAND BV HOLANDA |
| Models | 10216710153 |
| Date | Jun 23, 2016 |
| 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