International safety notice
Alert 2739 (Technosurveillance) - GE Healthcare do Brasil - Centricity Universal Viewer - Image orientation markers may be displayed incorrectly in certain scenarios when images are offset.
Brazil / Anvisa · BRA · Nov 27, 2018
Key facts
| Title | Alert 2739 (Technosurveillance) - GE Healthcare do Brasil - Centricity Universal Viewer - Image orientation markers may be displayed incorrectly in certain scenarios when images are offset. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade Name: Centricity Universal Viewer Technical Name: Software ANVISA registration number: 80071260349 Risk Class: II Affected model: Centricity Universal Viewer Zero Footprint Client Affected batch/serial numbers: HCIT4568867ZFP |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO GE HEALTHCARE DO BRASIL COM E SERV PARA EQUIPAMENTOS MÉDICOHOSPITALARES LTDA CNPJ 00029372000140 AV MAGALHÃES DE CASTRO Nº 4800 11º ANDAR CIDADE JARDIM SÃO PAULO SP TEL 11 30678436 EMAIL PATRICIASANTANAGECOM FABRICANTE DO PRODUTO GE HEALTHCARE 540 W NORTHWEST HIGHWAY BARRINGTON IL 60010 ESTADOS UNIDOS |
| Models | HCIT4568867ZFP, 80071260349 |
| Date | Nov 27, 2018 |
| 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