International safety notice
Technical name: LEKTRAFUSE HF GENERATOR BIPOLAR
Brazil / Anvisa · BRA · Dec 19, 2016
Key facts
| Title | Technical name: LEKTRAFUSE HF GENERATOR BIPOLAR |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Generators Technical name: LEKTRAFUSE HF GENERATOR BIPOLAR ANVISA registration number: 80136990815 Risk class: III Affected model: GN200 Affected serial numbers: 2028, 2054, 2060, 2065, 2066, 2071, 2070, 2072, 2074, 2075 , 2077, 2079, 2081, 2083, 2089, 2094, 2149, 2151, 2152, 2153, 2155, 2156, 2172. |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO LABORATÓRIOS B BRAUN SA AV EUGÊNIO BORGES 1092 E AV JEQUITIBÁ 9 CEP 24751000 RJ TELEFONE 55 21 26023219 FABRICANTE AESCULAP AG TUTTLINGEN AAG ALEMANHA AM AESCULAP PLATZ 78532 TUTTLINGEN 49 7461 95 31699 |
| Models | GN200, 80136990815 |
| Date | Dec 19, 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