International safety notice
Alert 2551 (Technosurveillance) Fresenius - Blood Line for Hemodialysis Possibility of rupture in the pump segment of the blood line.
Brazil / Anvisa · BRA · Apr 20, 2018
Key facts
| Title | Alert 2551 (Technosurveillance) Fresenius - Blood Line for Hemodialysis Possibility of rupture in the pump segment of the blood line. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Blood Line for Hemodialysis Technical name: Hemodialysis Equipment ANVISA registration number: 80133950083 Risk class: II Affected model: Arterial without catabola Affected Lot/Series Numbers: Lot: 03717, 07217, 07717, 08517 and 09417 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO FRESENIUS MEDICAL CARE LTDA CNPJ 01440590000136 RUA AMOREIRA 891 BAIRRO JARDIM ROSEIRA JAGUARIÚNA SP TEL 21 21792452 EMAIL VERAPEREIRAFMCAGCOM FABRICANTE AFRI MEDICAL COMPANY 13 OBOUR BUILDINGS SALAH SALEM STREET CAIRO EGITO |
| Models | 07717, 08517, 80133950083, 03717, 09417, 07217 |
| Date | Apr 20, 2018 |
| 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