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ANVISA registration 81931150020Active

SPERM DNA FRAGMENTATION

ANVISA Registration Number: 81931150020INTERMEDICAL SERVICE IMPORTACAO E EXPORTACAO DE EQUIPAMENTOS MEDICOS LTDABONRAYBIO CO., L TD.Risk Class II
Verified
Device names
Technical name
SPERM DNA FRAGMENTATION
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PT: FRAGMENTAÇÃO DO DNA ESPERMÁTICO
Commercial name
Kit de Teste Rápido de Fragmentação de DNA Dupla Hélice em Espermatozóides LensHooke® (Ensaio SDFR) R11 Plus
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Risk class
Class II
Registration details
Registration Number
81931150020
Process Number
25351033799202617
CNPJ
11205033000194
Company information
Registration Holder
INTERMEDICAL SERVICE IMPORTACAO E EXPORTACAO DE EQUIPAMENTOS MEDICOS LTDA
Manufacturer
BONRAYBIO CO., L TD.
Manufacturing Country
Taiwan
PT: TAIWAN
Dates and status
Publication Date
Apr 13, 2026
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for SPERM DNA FRAGMENTATION in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81931150020 and manufactured by BONRAYBIO CO., L TD.. The registration is held by INTERMEDICAL SERVICE IMPORTACAO E EXPORTACAO DE EQUIPAMENTOS MEDICOS 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.