International safety notice
Technical name: BLOOD BAG
Brazil / Anvisa · BRA · Jul 15, 2016
Key facts
| Title | Technical name: BLOOD BAG |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: CPDA-1 BLOOD COLLECTION BAG /// Technical name: BLOOD BAG /// ANVISA registration number: 10154450085 /// Risk class: III - High Risk /// Model: Triple Bag with DEHP Plasticizers and TOTM - Composampler /// Affected serial numbers: 71KA18AA00. |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO FRESENIUS HEMOCARE BRASIL LTDA CNPJ 49601107000184 RUA ROQUE GONZALES 128 ITAPECERICA DA SERRA SP TELEFONE 11 25041481 EMAIL CINTIAGARCIAFRESENIUSKABICOM FABRICANTE FRESENIUS HEMOCARE BRASIL LTDA CNPJ 49601107000184 RUA ROQUE GONZALES 128 ITAPECERICA DA SERRA SP TELEFONE 11 25041481 EMAIL CINTIAGARCIAFRESENIUSKABICOM |
| Models | 71KA18AA00, CPDA-1, 10154450085 |
| Date | Jul 15, 2016 |
| 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