International safety notice
MAGNETIC RESONANCE IMAGING SYSTEM
Brazil / Anvisa · BRA · Jun 21, 2016
Key facts
| Title | MAGNETIC RESONANCE IMAGING SYSTEM |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: MAGNETIC RESONANCE IMAGING SYSTEM (Model: DISCOVERY MR750W 3.0T) ANVISA registration number: 80071260134 Risk class: II Affected Serial No.(s): 00000309092MR5, 00000310904MR8, 00001301FMM03E, 00001309FMM072, and 00000000UA0467. |
| Manufacturer | NOME DA EMPRESA FABRICANTE GE MEDICAL SYSTEMS LLC PAÍS ESTADOS UNIDOS ENDEREÇO 3200 NORTH GRANDVIEW BOULEVARD WUAKESHA WISCONSIN 53188 |
| Models | 00001301FMM03E, 80071260134, MR750W, 00000309092MR5, 00000310904MR8, 00001309FMM072, 00000000UA0467 |
| Date | Jun 21, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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