ANVISA registration 82956209001Active

Removal Solution

Name: Removal Solution — ANVISA registration 82956209001
Creator: LABORATORIO HAZMAT SPA
Keywords: Removal Solution, Solucao Removedora, GPOLAROL, 82956209001, Risk Class II, ANVISA registration

ANVISA Registration Number: 82956209001KASEM BRASIL COMERCIAL LTDALABORATORIO HAZMAT SPARisk Class II

Verified

Device names

Technical name: Removal Solution
Commercial name: GPOLAROL
Risk class: Class II

Registration details

Registration Number: 82956209001
Process Number: 25351081657202658
CNPJ: 50849767000168

Company information

Registration Holder: KASEM BRASIL COMERCIAL LTDA
Manufacturer: LABORATORIO HAZMAT SPA
Manufacturing Country: Chile

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 Removal Solution in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82956209001 and manufactured by LABORATORIO HAZMAT SPA. The registration is held by KASEM BRASIL COMERCIAL 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.