International safety notice
Technical name: Surgical/Clinical Planning Software
Brazil / Anvisa · BRA · Dec 21, 2016
Key facts
| Title | Technical name: Surgical/Clinical Planning Software |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: iPlan Surgical/Clinical Planning Software, Brainlab and Brainscan brand Technical name: Surgical/Clinical Planning Software ANVISA registration number: 80042070008 Risk class: III |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO BRAINLAB LTDA ENDEREÇO RUA SABARÁ 566 CONJ 201 A 204 HIGIENÓPOLIS SP TELEFONE 11 33553371 FABRICANTE BRAINLAB AG ENDEREÇO KAPELLENSTRASSE 12 85622 FELDKIRCHEN TELEFONE 49 89 9915680 |
| Models | 80042070008 |
| Date | Dec 21, 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