International safety notice
Technical name: Family of Equipment for Gravitational Infusion of Parenteral Solutions and Medications
Brazil / Anvisa · BRA · Apr 13, 2017
Key facts
| Title | Technical name: Family of Equipment for Gravitational Infusion of Parenteral Solutions and Medications |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: INTRAFIX PRIMELINE AIR IL Technical name: Family of Equipment for Gravitational Infusion of Parenteral Solutions and medications ANVISA registration number: 80136990540 Risk class: II Affected model: 401450P Affected serial numbers: 17A20LB026 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO LABORATÓRIOS B BRAUN SA AV EUGÊNIO BORGES 1092 E AV JEQUITIBÁ 9 CEP 24751000 CEP 24751000 RJ BRASIL FABRICANTE LABORATÓRIOS B BRAUN SA AV EUGÊNIO BORGES 1092 E AV JEQUITIBÁ 9 CEP 24751000 CEP 24751000 RJ BRASIL |
| Models | 401450P, 80136990540, 17A20LB026 |
| Date | Apr 13, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
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