ANVISA registration 10407990091Valid until Apr 01, 2034CORONARY ANGIOPLASTY BALLOON CATHETER
ANVISA Registration Number: 10407990091ANGIOMED IMPORTACAO E EXPORTACAO LTDASIMEKS TIBBI URUNLER SANAYI VE TICARET LIMITED SIRKETIRisk Class IV
Device names
- Technical name
- CORONARY ANGIOPLASTY BALLOON CATHETER
- Commercial name
- Simvalve Flex - Cateter Balão para Valvuloplastia
- Risk class
- Class IV
PT: CATETER BALÃO PARA ANGIOPLASTIA CORONÁRIA
Registration details
- Registration Number
- 10407990091
- Process Number
- 25351120312202384
- CNPJ
- 02699256000164
Company information
- Registration Holder
- ANGIOMED IMPORTACAO E EXPORTACAO LTDA
- Manufacturing Country
- Türkiye
PT: TURQUIA
Dates and status
- Publication Date
- Apr 01, 2024
- Validity
- 01/04/2034
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for CORONARY ANGIOPLASTY BALLOON CATHETER in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 10407990091 and manufactured by SIMEKS TIBBI URUNLER SANAYI VE TICARET LIMITED SIRKETI. The registration is held by ANGIOMED IMPORTACAO E EXPORTACAO LTDA with validity until Apr 01, 2034.
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