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
- Commercial name
- SISTEMA DE STENT CORONÁRIO COM ELUIÇÃO DE SIROLIMUS ORSIRO MISSION
- Risk class
- Class IV
PT: STENT FARMACOLÓGICO PARA ARTÉRIAS CORONÁRIAS
Registration details
- Registration Number
- 80312270088
- Process Number
- 25351191149202504
- CNPJ
- 06089071000199
Company information
- Registration Holder
- TELEFLEX MEDICAL BRASIL LTDA
- 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.
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