International safety notice
Alert 2593 (Technosurveillance) - Philips Medical Systems Ltda - Allura Xper Angiography Equipment Philips brand Risk of monitor detachment and falling.
Brazil / Anvisa · BRA · Jun 26, 2018
Key facts
| Title | Alert 2593 (Technosurveillance) - Philips Medical Systems Ltda - Allura Xper Angiography Equipment Philips brand Risk of monitor detachment and falling. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade Name: Philips Brand Allura Xper Angiography Equipment Technical Name: Angiography Equipment ANVISA registration number: 10216710153 Risk Class: III Affected model: Allura Xper FD10 Affected serial numbers: 502, 947, 1143 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO PHILIPS MEDICAL SYSTEMS LTDA CNPJ 58295213000178 AV TAMBORÉ 14001440 BOX 31 A 33 TAMBORÉ BARUERI SÃO PAULO TEL 11 969109045 EMAIL LAISVIVONAPHILIPSCOM FABRICANTE DO PRODUTO PHILIPS MEDICAL SYSTEMS NEDERLAND BV VEENPLUIS 46 5684 PC BEST HOLANDA |
| Models | 10216710153 |
| Date | Jun 26, 2018 |
| 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