International safety notice
Alert 2629 (Technosurveillance) - Philips - Equip.
Brazil / Anvisa · BRA · Jul 26, 2018
Key facts
| Title | Alert 2629 (Technosurveillance) - Philips - Equip. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial Name: Philips Brand Allura Xper Angiography Equipment / Philips Brand Integris Allura Angiography Equipment Technical Name: Angiography Equipment ANVISA registration number: 10216710153 / 10216710155 Risk Class: III Affected model: Allura Xper FD10 and Allura Xper FD20; Números de série afetados: S4F200109; 566; 100034508; 393; 1105; 1109; 1522; 1568; 1569; 1570; 1639; 1620; 1726; 1751; 1743; 1702; 1255; 125; 555; 1402; 1923; 2043; 2117; 2389; 45; 53; 91; 123; 173; 176; 187; 289; 248; 231; 230; 232; 109; 180; 550; S01H055478; 49; 21; S4F000284; S01H060871; SN (Tech Id: CV0240); 440; S/N. (Tech Id: CV0246); S_N (Tech Id: CV0248); 426; 374. |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO PHILIPS MEDICAL SYSTEMS LTDA AV MARCOS PENTEADO DE ULHOA RODRIGUES 401 SETOR PARTE 39 TAMBORÉ BARUERI SÃO PAULO TEL 11 975763608 21250023 EMAIL LARISSAFRIASPHILIPSCOM FABRICANTE DO PRODUTO PHILIPS MEDICAL SYSTEMS NEDERLAND BV VEENPLUIS 46 5684 PC BEST HOLANDA HOLANDA |
| Models | 100034508, S4F200109, S01H060871, S01H055478, CV0246, CV0248, 10216710155, CV0240, 10216710153, S4F000284 |
| Date | Jul 26, 2018 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
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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.
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