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ANVISA registration 81313770058Active

Instrumento para preparo e processamento de amostras – fase pré-analítica

ANVISA Registration Number: 81313770058MEDMAX COMÉRCIO DE EQUIPAMENTOS MÉDICOS E SIMILARES LTDA MEJIANGSU XINKANG MEDICAL INSTRUMENTS CO., LTDRisk Class I
Verified
Device names
Technical name
Instrumento para preparo e processamento de amostras – fase pré-analítica
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Commercial name
FAMÍLIA DE CENTRÍFUGAS LABORATORIAIS SPIN MAX (80-2B/80-2B-1)
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Risk class
Class I
Registration details
Registration Number
81313770058
Process Number
25351389028202410
CNPJ
07760277000323
Company information
Registration Holder
MEDMAX COMÉRCIO DE EQUIPAMENTOS MÉDICOS E SIMILARES LTDA ME
Manufacturer
JIANGSU XINKANG MEDICAL INSTRUMENTS CO., LTD
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Nov 04, 2024
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Instrumento para preparo e processamento de amostras – fase pré-analítica in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81313770058 and manufactured by JIANGSU XINKANG MEDICAL INSTRUMENTS CO., LTD. The registration is held by MEDMAX COMÉRCIO DE EQUIPAMENTOS MÉDICOS E SIMILARES LTDA ME 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.