International safety notice
Technical name: Columbus rev.
Brazil / Anvisa · BRA · Nov 10, 2017
Key facts
| Title | Technical name: Columbus rev. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Atlas Gold Dilation Catheter Technical name: Columbus rev. ANVISA registration number: 80136990668 Risk class: III Affected model: NR586K/ NR587K Affected serial numbers: NR586K Code: 51586634 and 51447596; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO LABORATÓRIOS B BRAUN SA CNPJ 31673254000102 AV EUGÊNIO BORGES 1092 E AV JEQUITIBÁ 9 CEP 24751000 CHÁCARA SANTO ANTONIO SÃO GONÇALO RJ FABRICANTE AESCULAP AG SIEGFRIED SCHWARZ AM AESCULAPPLATZ D78532 TUTTLINGEN ALEMANHA TELEFONE 49 7461 95 1785 EMAIL DENISHOEFFGENAESCULAPDE |
| Models | 51585136, 51447596, post.f6, 80136990668, NR587K, NR586K, 51447597, 51586634 |
| Date | Nov 10, 2017 |
| 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