ANVISA registration 80785070285Active

LYSIS SOLUTION

Name: LYSIS SOLUTION — ANVISA registration 80785070285
Creator: Vida Biotecnologia Ltda - ME
Keywords: LYSIS SOLUTION, SOLUÇÃO DE LISE, VIDALISE 5 DIFF, 80785070285, Risk Class I, ANVISA registration

ANVISA Registration Number: 80785070285Vida Biotecnologia Ltda - MEVida Biotecnologia Ltda - MERisk Class I

Verified

Device names

Technical name: LYSIS SOLUTION
Commercial name: VIDALISE 5 DIFF
Risk class: Class I

Registration details

Registration Number: 80785070285
Process Number: 25351078531202604
CNPJ: 11308834000185

Company information

Registration Holder: Vida Biotecnologia Ltda - ME
Manufacturer: Vida Biotecnologia Ltda - ME
Manufacturing Country: Brazil

Dates and status

Publication Date: May 25, 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 80785070285 and manufactured by Vida Biotecnologia Ltda - ME. The registration is held by Vida Biotecnologia Ltda - ME 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.