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ANVISA registration 80312270088Valid until Jan 11, 2031

DRUG-ELUTING STENT FOR CORONARY ARTERIES

ANVISA Registration Number: 80312270088TELEFLEX MEDICAL BRASIL LTDABIOTRONIK AGRisk Class IV
Device names
Technical name
DRUG-ELUTING STENT FOR CORONARY ARTERIES
PT: STENT FARMACOLÓGICO PARA ARTÉRIAS CORONÁRIAS
Commercial name
SISTEMA DE STENT CORONÁRIO COM ELUIÇÃO DE SIROLIMUS – ORSIRO MISSION
Risk class
Class IV
Registration details
Registration Number
80312270088
Process Number
25351191149202504
CNPJ
06089071000199
Company information
Manufacturer
BIOTRONIK AG
Manufacturing Country
Switzerland
PT: SUÍÇA
Dates and status
Publication Date
Dec 22, 2025
Validity
11/01/2031
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for DRUG-ELUTING STENT FOR CORONARY 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 80312270088 and manufactured by BIOTRONIK AG. The registration is held by TELEFLEX MEDICAL BRASIL LTDA with validity until Jan 11, 2031.

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.