International safety notice
Technical name: Peripheral Intravenous Catheter
Brazil / Anvisa · BRA · Mar 24, 2017
Key facts
| Title | Technical name: Peripheral Intravenous Catheter |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Peripheral Intravenous Catheter Technical name: Peripheral Intravenous Catheter ANVISA registration number: 80288090083 Risk class: II Affected model: CIP01 - 24G - 0.7X19mm Affected batch/serial numbers: 160386/103 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO TKL IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS MÉDICOS E HOSPITALARES LTDA ENDEREÇO RUA ENGENHEIRO JÚLIO CESAR DE SOUZA ARAÚJO 220 CIDADE INDUSTRAIL CURITIBA PARANÁ TELEFONE 41 30220926 CNPJ 07415627000152 FABRICANTE DISPOSAFE HEALTH AND LIFECARE LTD ENDEREÇO PLOT Nº 1E 2 FASE II SETOR 59 BALLABGARH 121004 TELEFONE 91 129 4170201 4160201 |
| Models | 80288090083, CIP01, 160386 |
| Date | Mar 24, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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