International safety notice
Technical name: Surgical/Clinical Planning Software
Brazil / Anvisa · BRA · Oct 7, 2016
Key facts
| Title | Technical name: Surgical/Clinical Planning Software |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: iPlan Surgical/Clinical Planning Software, Brainlab brand /// Technical name: Surgical/Clinical Planning Software /// ANVISA registration number: 80042070008 /// Risk class: III - High Risk |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO BRAINLAB LTDA CNPJ 02981566000177 RUA SABARÁ 566 CONJ 201 A 204 HIGIENÓPOLIS SÃO PAULOSP FABRICANTE BRAINLAB AG KAPELLENSTRASSE 12 85622 FELDKIRCHEN ALEMANHA |
| Models | 80042070008 |
| Date | Oct 7, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 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