ANVISA registration 81576629024ActivePERIPHERAL ANGIOPLASTY BALLOON CATHETER
ANVISA Registration Number: 81576629024CORDIS MEDICAL BRASIL LTDACORDIS CASHELRisk Class II
Device names
- Technical name
- PERIPHERAL ANGIOPLASTY BALLOON CATHETER
- Commercial name
- Cateter de Dilatação para Angioplastia Transluminal Percutânea (PTA) SABERX RADIANZ
- Risk class
- Class II
PT: CATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA
Registration details
- Registration Number
- 81576629024
- Process Number
- 25351110897202413
- CNPJ
- 27548227000122
Company information
- Registration Holder
- CORDIS MEDICAL BRASIL LTDA
- Manufacturer
- CORDIS CASHEL
- Manufacturing Country
- Ireland
PT: IRLANDA
Dates and status
- Publication Date
- Mar 25, 2024
- Validity
- VIGENTE
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for PERIPHERAL ANGIOPLASTY BALLOON CATHETER in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81576629024 and manufactured by CORDIS CASHEL. The registration is held by CORDIS MEDICAL BRASIL LTDA with validity until currently active (VIGENTE).
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