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ANVISA registration 80102511476Active

Laser Device For Ophthalmic Diagnosis

ANVISA Registration Number: 80102511476VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDAHAAG-STREIT AGRisk Class II
Verified
Device names
Technical name
Laser Device For Ophthalmic Diagnosis
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PT: Aparelho a Laser Para Diagnostico Oftalmologico
Commercial name
Biômetro LENSTAR 900
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Risk class
Class II
Registration details
Registration Number
80102511476
Process Number
25351372914201514
CNPJ
04718143000194
Company information
Registration Holder
VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA
Manufacturer
HAAG-STREIT AG
Manufacturing Country
Switzerland
PT: SUÍÇA
Dates and status
Publication Date
Aug 10, 2015
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Laser Device For Ophthalmic Diagnosis in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80102511476 and manufactured by HAAG-STREIT AG. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS 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.