International safety notice
Alert 2780 (Technosurveillance) - Philips Medical Systems Ltda Magnetic Resonance Equipment - Intera;
Brazil / Anvisa · BRA · Jan 18, 2019
Key facts
| Title | Alert 2780 (Technosurveillance) - Philips Medical Systems Ltda Magnetic Resonance Equipment - Intera; |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial Name: Magnetic Resonance Equipment - Intera; Technical Name: Magnetic Resonance Equipment ANVISA registration numbers: 10216710194; Risk Class: III Affected model: Intera 1.0T, Intera 1.5 T (10216710194); Affected serial numbers: See attachment List of batches/series at risk |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO PHILIPS MEDICAL SYSTEMS LTDA CNPJ 58295213000178 AV TAMBORÉ 14001440 BOX 31 A 33 TAMBORÉ BARUERI SÃO PAULO TEL 11 995576799 EMAIL TECNOVIGILANCIABRPHILIPSCOM FABRICANTE DO PRODUTO PHILIPS MEDICAL SYSTEMS NEDERLAND BV VEENPLUIS 46 5584 PC BEST HOLANDA |
| Models | 10216710293, 10216710351, 10216710205, 10216710217, 10216710194 |
| Date | Jan 18, 2019 |
| 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