International safety notice
Probes
Brazil / Anvisa · BRA · Jun 10, 2015
Key facts
| Title | Probes |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Probes for ophthalmological equipment, Accurus 2500 Probe model, registration 80153480154 and Accurus 23 Gauge Probe model, registration 80153480154. Risk class II. |
| Manufacturer | DETENTOR DO REGISTRO NOVARTIS BIOCIÊNCIAS CNPJ 56994502000130 ENDEREÇO AVENIDA PROFESSOR VICENTE RAO 90 SÃO PAULOSP FABRICANTE ALCON LABORATORIES INC ENDEREÇO 6201 SOUTH FREEWAY FORT WORTH TEXAS |
| Models | 14017912X, 14031263X, 14012987X, 80153480154, 15010057X, 14033830X, 14022920X, 14014736X, 14010428X, 14016577X, 14026031X, 14026030X and 4 more |
| Date | Jun 10, 2015 |
| 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