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ANVISA registration 81596320085Active

SPACER

ANVISA Registration Number: 81596320085GRUPO MULTILASER S.A.SHENZHEN HOMED MEDICAL DEVICE CO., LTD.Risk Class I
Verified
Device names
Technical name
SPACER
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PT: ESPAÇADOR
Commercial name
ESPAÇADOR PARA MEDICAMENTOS DE ASMA
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Risk class
Class I
Registration details
Registration Number
81596320085
Process Number
25351148411202321
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
Mar 20, 2023
Status
Active
Official value: VIGENTE
About this record

Access comprehensive regulatory information for SPACER in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81596320085 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.