International safety notice
Technical Name: Agglutination Reactions Reader - Risk Class: I - LOW RISK - Product Name: LYRA II AGLUTINATION REACTIONS READER - Registration: 80004040165
Brazil / Anvisa · BRA · Jul 27, 2015
Key facts
| Title | Technical Name: Agglutination Reactions Reader - Risk Class: I - LOW RISK - Product Name: LYRA II AGLUTINATION REACTIONS READER - Registration: 80004040165 |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Product Name: LYRA II AGLUTINATION REACTION READER - Registration: 80004040165 - Model: 854002 - Affected batches/series: 407;422; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO NO BRASIL DIAMED LATINO AMÉRICA SA CNPJ 71015853000145 RUA ALFREDO ALBANO DA COSTA 100 DISTRITO INDUSTRIAL LAGOA SANTAMG EMPRESA FABRICANTE DIAMED GMBH PRA ROND 23 1785 SUÍÇA |
| Models | 854002, LY1B000402, LY3F007308, LY3F007303, 80004040165, LY0K000303, LY1B000409, LY2C003904, LYB000407, LY0K000306, LY1B000401, LY0K000305 and 9 more |
| Date | Jul 27, 2015 |
| 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