International safety notice
Laser equipment for ophthalmology
Brazil / Anvisa · BRA · Apr 26, 2016
Key facts
| Title | Laser equipment for ophthalmology |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name of the product: LENSX LASER SYSTEM /// Registration number: 80153480158 /// Affected serial number: 0413-A364; |
| Manufacturer | DETENTOR DO REGISTRO NOVARTIS BIOCIÊNCIAS ENDEREÇO AVENIDA PROFESSOR VICENTE RAO 90 SÃO PAULO SP TEL 11 37324023 FABRICANTES ALCON LABORATORIES INC ENDEREÇO 6201 SOUTH FREEWAY FORT WORTH TEXAS EUA |
| Models | 0414-A727, 80153480158, 0714-A808, 1213-A621, 0413-A364, 1213-A620, 0714-A802, 1013-A535, 0713-A450, 1213-A622 |
| Date | Apr 26, 2016 |
| 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