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ANVISA registration 10371280047Active

ENDOSCOPY SYSTEM

ANVISA Registration Number: 10371280047PENTAX MEDICAL BRASIL MATERIAIS E EQUIPAMENTOS LTDA - EPPPENTAX - AOHUA MEDICAL TECHNOLOGIES CO., LTD.Risk Class II
Verified
Device names
Technical name
ENDOSCOPY SYSTEM
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PT: SISTEMA DE ENDOSCOPIA
Commercial name
Videoendoscópio Gastroscópio Inferior PENTAX Medical
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Risk class
Class II
Registration details
Registration Number
10371280047
Process Number
25351559238201914
CNPJ
01716863000122
Company information
Registration Holder
PENTAX MEDICAL BRASIL MATERIAIS E EQUIPAMENTOS LTDA - EPP
Manufacturer
PENTAX - AOHUA MEDICAL TECHNOLOGIES CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Dec 23, 2019
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for ENDOSCOPY 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 10371280047 and manufactured by PENTAX - AOHUA MEDICAL TECHNOLOGIES CO., LTD.. The registration is held by PENTAX MEDICAL BRASIL MATERIAIS E EQUIPAMENTOS LTDA - EPP 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.