International safety notice
Alert 2666 (Technovigilance) - TKL Importação e Exportação de Produtos Médicos e Hospitalares Ltda.
Brazil / Anvisa · BRA · Sep 5, 2018
Key facts
| Title | Alert 2666 (Technovigilance) - TKL Importação e Exportação de Produtos Médicos e Hospitalares Ltda. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade Name: Peripheral Intravenous Catheter Technical Name: Catheters ANVISA registration number: 80288090083 Risk Class: II Affected model: CIP 01 - 18G, 20G, 22G Affected lots: 170662/216, 170048/010, 170282/088 and 171018/334 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO TKL IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS MÉDICOS E HOSPITALARES LTDA CNPJ 07415627000152 RUA ENGENHEIRO JÚLIO CÉSAR DE SOUZA ARAÚJO Nº 220 CIC CURITIBA PARANÁ TEL 04130220926 EMAIL KELENTKLBRASILCOMBR FABRICANTE DO PRODUTO DISPOSAFE HEALTH AND LIFECARE LTD PLOT Nº 1E 2 FASE II SETOR 59 BALLABGARH 121004 ÍNDIA |
| Models | 80288090083, 171018, 170048, 170282, 170662 |
| Date | Sep 5, 2018 |
| 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