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ANVISA registration 80102513407Valid until Apr 14, 2035

CARDIOVASCULAR GUIDE WIRE

ANVISA Registration Number: 80102513407VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDALIFETECH SCIENTIFIC (SHENZHEN) CO., LTD.Risk Class IV
Verified
Device names
Technical name
CARDIOVASCULAR GUIDE WIRE
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PT: FIO GUIA CARDIOVASCULAR
Commercial name
Fio-guia Super Stiff ZoeTrack™
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Risk class
Class IV
Registration details
Registration Number
80102513407
Process Number
25351346066202470
CNPJ
04718143000194
Company information
Registration Holder
VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA
Manufacturer
LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Apr 14, 2025
Validity
14/04/2035
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for CARDIOVASCULAR GUIDE WIRE in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80102513407 and manufactured by LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD.. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Apr 14, 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.