International safety notice
Centrifuge.
Brazil / Anvisa · BRA · May 2, 2012
Key facts
| Title | Centrifuge. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | LS 3 PLUS CENTRIFUGE (ANVISA Registration No. 80197039010), affected batch: 110116 (series: 2178 to 2227). COMBATE CENTRIFUGE (ANVISA Registration No. 80197039011), affected lots: 100804 and 110115 (series: 6334 to 6391). |
| Manufacturer | FABRICANTEDETENTOR DE REGISTRO CELM CIA EQUIPADORA DE LABORATORIOS MODERNOS CNPJ 61086823000176 END ALAMEDA AMAZONAS 764 ALPHAVILLE INDUSTRIAL BARUERI SP TELFAX 11 41335200 11 41335211 EMAIL LUCIANAVEIGACELMCOMBR |
| Models | 100804, 80197039010, 80197039011, 110116, 110115 |
| Date | May 2, 2012 |
| 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