International safety notice
Diagnostic kit
Brazil / Anvisa · BRA · Nov 3, 2014
Key facts
| Title | Diagnostic kit |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Immuno-Hemato Anti-A and Anti-B diagnostic kit, Risk Class IV, Model: COD 1054010-AB/1054100- AB, Brand: WAMA Produtos para Laboratórios LTDA., Registration: 10310030159, Affected lots: 14D045/ 14D046 / 14E055 / 14E058 / 14H123 / 14H126. Immuno-Hemato Anti-D diagnostic kit, Risk Class IV, Model: COD1055010-D/1055100-D, Brand: WAMA Produtos para Laboratórios LTDA., Registration: 10310030161, Affected lots: 14D048/ 14D048R / 14H044 / 14E060. |
| Manufacturer | DETENTOR DO REGISTRO E FABRICANTE WAMA PRODUTOS PARA LABORATÓRIOS LTDA CNPJ 66000787000108 ENDEREÇO RUA ALDO GERMANO KLEIN 100 CEAT |
| Models | 14E060, COD1055010-D, 14D045, 1054100, 1055100-D, 14D046, 10310030159, 14D048R, 14E058, 14H126, 1054010-AB, 14H123 and 4 more |
| Date | Nov 3, 2014 |
| 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