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ANVISA registration 81487660006Valid until Oct 24, 2035

DRUG-ELUTING STENT FOR PERIPHERAL ARTERIES

ANVISA Registration Number: 81487660006GF MEDIKA IMPORTAÇÃO E EXPORTAÇÃO LTDAZYLOX-TONBRIDGE MEDICAL TECHNOLOGY CO., LTD.Risk Class IV
Verified
Device names
Technical name
DRUG-ELUTING STENT FOR PERIPHERAL ARTERIES
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PT: STENT FARMACOLÓGICO PARA ARTÉRIAS PERIFÉRICAS
Commercial name
ZENFlex ProTM Sistema de Stent
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Risk class
Class IV
Registration details
Registration Number
81487660006
Process Number
25351391534202461
CNPJ
20503395000152
Company information
Registration Holder
GF MEDIKA IMPORTAÇÃO E EXPORTAÇÃO LTDA
Manufacturer
ZYLOX-TONBRIDGE MEDICAL TECHNOLOGY CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Oct 24, 2025
Validity
24/10/2035
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for DRUG-ELUTING STENT FOR PERIPHERAL ARTERIES in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 81487660006 and manufactured by ZYLOX-TONBRIDGE MEDICAL TECHNOLOGY CO., LTD.. The registration is held by GF MEDIKA IMPORTAÇÃO E EXPORTAÇÃO LTDA with validity until Oct 24, 2035.

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.