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ANVISA registration 83085839001Active

Assisted reproduction laser system

ANVISA Registration Number: 83085839001VITROLIFE BRASIL COMERCIO DE EQUIPAMENTOS LABORATORIAIS LTDAVITROLIFE GMBHRisk Class II
Verified
Device names
Technical name
Assisted reproduction laser system
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PT: Sistema de laser de reprodução assistida
Commercial name
Octax Laser
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Risk class
Class II
Registration details
Registration Number
83085839001
Process Number
25351079365202574
CNPJ
54416180000116
Company information
Registration Holder
VITROLIFE BRASIL COMERCIO DE EQUIPAMENTOS LABORATORIAIS LTDA
Manufacturer
VITROLIFE GMBH
Manufacturing Country
Germany
PT: ALEMANHA
Dates and status
Publication Date
Jun 16, 2025
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Assisted reproduction laser system in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 83085839001 and manufactured by VITROLIFE GMBH. The registration is held by VITROLIFE BRASIL COMERCIO DE EQUIPAMENTOS LABORATORIAIS 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.