International safety notice
Alert 2913 (Technosurveillance) - Fresenius - Orquestra Intensive Base (product accessory Linear Infusion Pump MVP Module) Possibility of technical alarm on the Orchestra Base in relation to a programmed channel relay.
Brazil / Anvisa · BRA · Jun 17, 2019
Key facts
| Title | Alert 2913 (Technosurveillance) - Fresenius - Orquestra Intensive Base (product accessory Linear Infusion Pump MVP Module) Possibility of technical alarm on the Orchestra Base in relation to a programmed channel relay. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial Name: Orquestra Intensive Base (product accessory Linear Infusion Pump MVP Module) Technical Name: Infusion Pump ANVISA registration number: 80145110219 Risk Class: III Affected model: MVP Module Linear Infusion Pump Affected serial numbers: Code BRZ081243CO. |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO FRESENIUS KABI BRASIL LTDA CNPJ 49324221000104 AV MARGINAL PROJETADA 1652 BARUERI SP TEL 11 25041481 EMAIL CINTIAGARCIAFRESENIUSKABICOM FABRICANTE DO PRODUTO FABRICANTE FRESENIUS VIAL SA LE GRAND CHEMIN 38590 BRÉZINS FRANÇA |
| Models | BRZ081243CO, 80145110219 |
| Date | Jun 17, 2019 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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