Pure Global AI
ANVISA registration 81826160104Active

LYSIS SOLUTION

ANVISA Registration Number: 81826160104ERBA DIAGNOSTICS BRAZIL, PRODUCAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDAERBA LACHEMA S.R.ORisk Class I
Verified
Device names
Technical name
LYSIS SOLUTION
View exact technical-name matches →
PT: SOLUÇÃO DE LISE
Commercial name
Erba H7100 Lyse1
View exact commercial-name matches →
Risk class
Class I
Registration details
Registration Number
81826160104
Process Number
25351237914202531
CNPJ
32190515000198
Company information
Registration Holder
ERBA DIAGNOSTICS BRAZIL, PRODUCAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDA
Manufacturer
ERBA LACHEMA S.R.O
Manufacturing Country
Czechia
PT: TCHECA, REPÚBLICA
Dates and status
Publication Date
Feb 09, 2026
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for LYSIS SOLUTION in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81826160104 and manufactured by ERBA LACHEMA S.R.O. The registration is held by ERBA DIAGNOSTICS BRAZIL, PRODUCAO E DISTRIBUICAO DE PRODUTOS MEDICOS 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.