International safety notice
Technical name: Scheimpflug analyzer for ophthalmology
Brazil / Anvisa · BRA · Dec 19, 2017
Key facts
| Title | Technical name: Scheimpflug analyzer for ophthalmology |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Pentacam Technical name: Scheimpflug analyzer for ophthalmology ANVISA registration number: 80039200010 Risk class: II Affected model: Pentacam, Pentacam HR and Pentacam AXL Affected serial numbers: 70100 0041 7160 70100 3121 6190 70100 5121 6190 70100 7611 6170 70100 0511 6170 70100 3611 6170 70100 5221 6101 70100 8221 6101 70100 1321 6101 70100 4021 6190 70100 5231 7130 70100 8521 6111 70100 1711 6170 70100 4321 6101 70100 6211 6150 70100 1931 7150 70100 4811 6190 70100 7121 6190 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO TECNICALL COMÉRCIO IMPORTAÇÃO E EXPORTAÇÃO LTDA CNPJ 01134078000161 RUA MARIA SALINA ROMEU 456 SÃO PAULO SP FABRICANTE OCULUS OPTIKGERÄTE GMBH MÜNCHHOLZHÄUSER STRASSE 29 35582 WETZLAR ALEMANHA TELEFONE 49 641 2005 255 EMAIL EXPORTOCULUSDE |
| Models | 80039200010, 70100 |
| Date | Dec 19, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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