International safety notice
IMMUNOHEMATOLOGY - RARE SERA FOR SPINE TECHNOLOGY
Brazil / Anvisa · BRA · Apr 15, 2016
Key facts
| Title | IMMUNOHEMATOLOGY - RARE SERA FOR SPINE TECHNOLOGY |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name of the product: ID-DiaClon Anti-N (MNS2) and ID-DiaClon Anti-M/-N/// Registration number: 80004040126/// Batches: 50221.73.01 and 50221.73.03 (D-DiaClon Anti- N (MNS2) (REF 007111))/// Product risk class: III. |
| Manufacturer | DETENTOR DO REGISTRO DIAMED LATINO AMÉRICA SA CNPJ 71015853000145 ENDEREÇO RUA ALFREDO ALBANO DA COSTA 100 DISTRITO INDUSTRIAL LAGOA SANTA MINAS GERAIS TELEFONE 31 36896613 FABRICANTE DIAMED GMBH ENDEREÇO PRA ROND 23 1785 CRESSIER FR SUIÇA |
| Models | 007111, 50221.73.01, 80004040126, 50221.73.03 |
| Date | Apr 15, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
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