International safety notice
IMUNO-LATEX FR/RHEUMATOID FACTOR (2.5 ml) # Technical name: RHEUMATOID FACTOR # Registration: 10310030088 # Risk Class: II - Products that present medium risk to the user or patient and low risk to public health
Brazil / Anvisa · BRA · Jul 4, 2014
Key facts
| Title | IMUNO-LATEX FR/RHEUMATOID FACTOR (2.5 ml) # Technical name: RHEUMATOID FACTOR # Registration: 10310030088 # Risk Class: II - Products that present medium risk to the user or patient and low risk to public health |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | # Commercial name: IMUNO-LATEX FR/RHEUMATOID FACTOR # COD. |
| Manufacturer | WAMA PRODUTOS PARA LABORATORIO LTDA CNPJ 66000787000108 ENDEREÇO RUA ALDO GERMANO KLEIN 100 CEAT SÃO CARLOS SP EMAIL ATENDIMENTOWAMADIAGNOSTICACOMBR |
| Models | 2800L, 10310030088 |
| Date | Jul 4, 2014 |
| 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