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ANVISA registration 80420209009Active

Dispositivo para implantação de lentes intra oculares

ANVISA Registration Number: 80420209009VISION LINE IMPORTAÇÃO E COMÉRCIO DE MATERIAIS E EQUIPAMENTOS MÉDICOS LTDA-MEAUROLABRisk Class II
Verified
Device names
Technical name
Dispositivo para implantação de lentes intra oculares
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Commercial name
GLIDE – Cartucho e injetor descartável
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Risk class
Class II
Registration details
Registration Number
80420209009
Process Number
25351553200202144
CNPJ
05187817000134
Company information
Registration Holder
VISION LINE IMPORTAÇÃO E COMÉRCIO DE MATERIAIS E EQUIPAMENTOS MÉDICOS LTDA-ME
Manufacturer
AUROLAB
Manufacturing Country
India
PT: ÍNDIA
Dates and status
Publication Date
Oct 28, 2021
Status
Active
Official value: VIGENTE
About this record

Access comprehensive regulatory information for Dispositivo para implantação de lentes intra oculares in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80420209009 and manufactured by AUROLAB. The registration is held by VISION LINE IMPORTAÇÃO E COMÉRCIO DE MATERIAIS E EQUIPAMENTOS MÉDICOS 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.