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ANVISA registration 80290739004Active

Incision Device

ANVISA Registration Number: 80290739004ENDOTECH COMERCIO IMPORTAÇÃO EXPORTAÇÃO E SERVIÇOS LTDASUZHOU FRANKENMAN MEDICAL EQUIPMENT CO., LTDRisk Class II
Verified
Device names
Technical name
Incision Device
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PT: Dispositivo para Incisão
Commercial name
OCTOport
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Risk class
Class II
Registration details
Registration Number
80290739004
Process Number
25351026734202526
CNPJ
03704024000110
Company information
Registration Holder
ENDOTECH COMERCIO IMPORTAÇÃO EXPORTAÇÃO E SERVIÇOS LTDA
Manufacturer
SUZHOU FRANKENMAN MEDICAL EQUIPMENT CO., LTD
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Mar 05, 2025
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Incision 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 80290739004 and manufactured by SUZHOU FRANKENMAN MEDICAL EQUIPMENT CO., LTD. The registration is held by ENDOTECH COMERCIO IMPORTAÇÃO EXPORTAÇÃO E SERVIÇOS 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.