International safety notice
AEO - Látex
Brazil / Anvisa · BRA · Jul 27, 2017
Key facts
| Title | AEO - Látex |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: AEO - Latex Technical name: AEO - Latex ANVISA registration number: 80022230177 Risk class: II Affected model: In vitro diagnostic kit Affected serial numbers: Cat. 541 - 7033 - manufactured (04/06/17 - validity: 01/31/19) = 231 kits Cat. 541L - 7053 - manufactured (05/22/17 - validity: 05/30/19) = 450 kits Cat. 541 - 7062 - manufactured (06/16/17 - validity: 01/31/19) = 150 kits |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO GOLD ANALISA DIAGNÓSTICA LTDA CNPJ 03142794000116 AVENIDA NOSSA SENHORA DE FÁTIMA 2363 E 2373 BAIRRO CARLOS PRATES BELO HORIZONTE MG FABRICANTE GOLD ANALISA DIAGNÓSTICA LTDA AVENIDA NOSSA SENHORA DE FÁTIMA 2363 E 2373 BAIRRO CARLOS PRATES BRASIL EMAIL QUALIDADEGOLDANALISACOMBR TELEFONE 3132721888 |
| Models | 80022230177 |
| Date | Jul 27, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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