International safety notice
Technical name: Catheter
Brazil / Anvisa · BRA · Nov 1, 2017
Key facts
| Title | Technical name: Catheter |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Hemodialysis Catheter - Eagle Flow Technical name: Catheter ANVISA registration number: 80120820020 Risk class: IV Affected model: HMP-3-20-SSK Affected serial numbers: 1612031; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO BIOLINE COMERCIAL LTDA CNPJ 04762934000111 RUA JOSÉ GETÚLIO 579 ANDAR 111314 ACLIMAÇÃO CEP 01509001 SÃO PAULOSP FABRICANTE HEALTH LINE INTERNATIONAL CORPORATION 5675 WEST 300 SOUTH SALT LAKE CITY UTAH 84104 USA EMAIL CUSTOMERSERVICEHLICNET TELEFONE 18778474542 |
| Models | 1612018, 80120820020, HMP-3-20-SSK, 1612031 |
| Date | Nov 1, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 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