International safety notice
Technical name: CENTRAL VENOUS CATHETER FAMILY
Brazil / Anvisa · BRA · Mar 3, 2017
Key facts
| Title | Technical name: CENTRAL VENOUS CATHETER FAMILY |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: CERTOFIX DUO V 720 JUG 7F and CERTOFIX DUO V 730 SUB 7F Technical name: FAMILY OF CENTRAL VENOUS CATHETERS ANVISA registration number: 80136990671 Risk class: IV Affected model: 4161211 and 4161319 Affected serial numbers: 16M15A8551 and 16M21A8551 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO LABORATÓRIOS B BRAUN SA ENDEREÇO AV EUGÊNIO BORGES 1092 E AV JEQUITIBÁ 9 CEP 24751000 TELEFONE 55 21 26023219 FABRICANTE B BRAUN MELSUNGEN AG ALEMANHA 34209 MELSUNGEN 05661 712769 |
| Models | 16M15A8551, 4161211, 80136990671, 4161319, 16M21A8551 |
| Date | Mar 3, 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