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ANVISA registration 80202910088Active

Dissection Device

ANVISA Registration Number: 80202910088TECMEDIC COMÉRCIO DE PRODUTOS MÉDICOS LTDALEMAITRE VASCULAR INCRisk Class II
Verified
Device names
Technical name
Dissection Device
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PT: Dispositivo Para Disseccao
Commercial name
Dispositivo para Dissecação/Transecção MultiTASC
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Risk class
Class II
Registration details
Registration Number
80202910088
Process Number
25351492036201603
CNPJ
05638301000169
Company information
Registration Holder
TECMEDIC COMÉRCIO DE PRODUTOS MÉDICOS LTDA
Manufacturer
LEMAITRE VASCULAR INC
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
May 17, 2017
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Dissection Device in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80202910088 and manufactured by LEMAITRE VASCULAR INC. The registration is held by TECMEDIC COMÉRCIO 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.