International safety notice
Alert 2619 (Technosurveillance) - GE Healthcare do Brasil, Com. and Serv.
Brazil / Anvisa · BRA · Jul 18, 2018
Key facts
| Title | Alert 2619 (Technosurveillance) - GE Healthcare do Brasil, Com. and Serv. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade Name: Magnetic Resonance Imaging System Technical Name: Magnetic Resonance Equipment ANVISA registration number: 80071260134 Risk Class: II Affected model: Discovery MR750w 3.0T Affected serial numbers: 00000309092MR5; |
| 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 TECNOVIGILANCIABRASILGECOM FABRICANTE DO PRODUTO GE MEDICAL SYSTEMS LLC 3200 NORTH GRANDVIEW BOULEVARD WUAKESHA WISCONSIN 53188 ESTADOS UNIDOS |
| Models | MR750w, 00000310904MR8, PG75W1600012MR, 00000000UA0467, 80071260134, 00001309FMM072, 00001301FMM03E, 00000309092MR5 |
| Date | Jul 18, 2018 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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