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ANVISA registration 81596329025Active

General purpose surgical suction pump, vacuum

ANVISA Registration Number: 81596329025GRUPO MULTILASER S.A.SHENZHEN HOMED MEDICAL DEVICE CO., LTD.Risk Class II
Verified
Device names
Technical name
General purpose surgical suction pump, vacuum
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PT: Bomba de sucção cirúrgica de uso geral, vácuo
Commercial name
Aspirador Cirúrgico Para fluídos das vias aéreas
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Risk class
Class II
Registration details
Registration Number
81596329025
Process Number
25351330877202114
CNPJ
59717553000102
Company information
Registration Holder
GRUPO MULTILASER S.A.
Manufacturer
SHENZHEN HOMED MEDICAL DEVICE CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Sep 23, 2021
Status
Active
Official value: VIGENTE
About this record

Access comprehensive regulatory information for General purpose surgical suction pump, vacuum in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81596329025 and manufactured by SHENZHEN HOMED MEDICAL DEVICE CO., LTD.. The registration is held by GRUPO MULTILASER S.A. 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.