ANVISA registration 80076800014Valid until Dec 30, 2029INTRAVASCULAR GUIDE CATHETER
ANVISA Registration Number: 80076800014ARTMÉDICA - PRODUTOS MÉDICOS E HOSPITALARES LTDAVASCULAR INNOVATIONS CO., LTDRisk Class IV
Device names
- Technical name
- INTRAVASCULAR GUIDE CATHETER
- Commercial name
- HYDRA18F HYDRA AORTIC VALVE DELIVERY SYSTEM (AVDC)
- Risk class
- Class IV
PT: CATETER GUIA INTRAVASCULAR
Registration details
- Registration Number
- 80076800014
- Process Number
- 25351274602201961
- CNPJ
- 03950712000160
Company information
- Registration Holder
- ARTMÉDICA - PRODUTOS MÉDICOS E HOSPITALARES LTDA
- Manufacturer
- VASCULAR INNOVATIONS CO., LTD
- Manufacturing Country
- Thailand
PT: TAILÂNDIA, REINO DA
Dates and status
- Publication Date
- Dec 30, 2019
- Validity
- 30/12/2029
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for INTRAVASCULAR GUIDE 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 80076800014 and manufactured by VASCULAR INNOVATIONS CO., LTD. The registration is held by ARTMÉDICA - PRODUTOS MÉDICOS E HOSPITALARES LTDA with validity until Dec 30, 2029.
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