International safety notice
PRODUCT: Double Lumen Catheter for Hemodialysis PALINDROME HSI //// REGISTRATION: 10349000341 ////RISK CLASS 4 (Maximum Risk)//// TECHNICAL NAME: Catheters
Brazil / Anvisa · BRA · May 11, 2015
Key facts
| Title | PRODUCT: Double Lumen Catheter for Hemodialysis PALINDROME HSI //// REGISTRATION: 10349000341 ////RISK CLASS 4 (Maximum Risk)//// TECHNICAL NAME: Catheters |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | PRODUCT: Double Lumen Catheter for Hemodialysis PALINDROME HSI //// REGISTRATION: 10349000341 ////RISK CLASS 4 (Maximum Risk) //// MODELS: 8888145048;8888145049;8888145050;8888145057 //// LOTS (See ANNEX) |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL AUTO SUTURE DO BRASIL LTDA CNPJ 01645409000128 ENDEREÇO AVENIDA JORNALISTA ROBERTO MARINHO 85 SÃO PAULOSP FABRICANTE COVIDIEN LLC ENDERECO 15 HAMPSHIRE STREET MANSFIELD MA CÓDIGO POSTAL 02048 ESTADOS UNIDOS |
| Models | 8888145050, 10349000341, 8888145049, 8888145057, 8888145048 |
| Date | May 11, 2015 |
| 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