ANVISA registration 80003610621ActiveSOLUÇÃO PARA AVALIAÇÃO DE DESEMPENHO DOS COMPONENTES DE EQUIPAMENTOS
ANVISA Registration Number: 80003610621WERFEN MEDICAL LTDALUMINEX CORPORATIONRisk Class I
Device names
- Technical name
- SOLUÇÃO PARA AVALIAÇÃO DE DESEMPENHO DOS COMPONENTES DE EQUIPAMENTOS
- Risk class
- Class I
Registration details
- Registration Number
- 80003610621
- Process Number
- 25351162226202519
- CNPJ
- 02004662000165
Company information
- Registration Holder
- WERFEN MEDICAL LTDA
- Manufacturer
- LUMINEX CORPORATION
- Manufacturing Country
- United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
- Publication Date
- Oct 24, 2025
- Validity
- VIGENTE
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for SOLUÇÃO PARA AVALIAÇÃO DE DESEMPENHO DOS COMPONENTES DE EQUIPAMENTOS in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80003610621 and manufactured by LUMINEX CORPORATION. The registration is held by WERFEN MEDICAL LTDA with validity until currently active (VIGENTE).
This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.