International safety notice
Alert 2912 (Technosurveillance) Bard do Brasil Equistream and Equistream
Brazil / Anvisa · BRA · Jun 17, 2019
Key facts
| Title | Alert 2912 (Technosurveillance) Bard do Brasil Equistream and Equistream |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial Name: Equistream (registration 80689090050); Technical Name: Catheters ANVISA registration number: 80689090050; Risk Class: III Affected model: Registration 80689090050 - Equistream - Models: 6903190, 6903230, 6903270, 6903310, 6903350, 6903420, 6905280. / Registration 80689090063 Equistream XK Model: 6913350. Affected serial numbers: Catalog 6903190, Lots RECX1116, RECX1473; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO BARD DO BRASIL INDUSTRIA E COMÉRCIO DE PRODUTOS PARA SAÚDE LTDA CNPJ 10818693000188 RUA ALEXANDRE DUMAS 2100 10 ANDAR CHACARA SANTO ANTONIO SÃO PAULO SP TEL 11 5185 9990 EMAIL BRCRBDCOM FABRICANTE DO PRODUTO BARD ACCESS SYSTEMS INC 605 NORTH 5600 WEST SALT LAKE CITY UTAH EUA |
| Models | RECZ1124, RECX1473, RECW0906, RECX2829, 80689090050, 6905280, 6903270, 6903310, 6903350, RECW2017, RECX2700, RECZ3013 and 10 more |
| Date | Jun 17, 2019 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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