ANVISA registration 80202910112Valid until Jul 07, 2035PERIPHERAL ANGIOPLASTY BALLOON CATHETER
ANVISA Registration Number: 80202910112TECMEDIC COMÉRCIO DE PRODUTOS MÉDICOS LTDAAR BALTIC MEDICAL UABRisk Class IV
Device names
- Technical name
- PERIPHERAL ANGIOPLASTY BALLOON CATHETER
- Risk class
- Class IV
PT: CATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA
Registration details
- Registration Number
- 80202910112
- Process Number
- 25351391217202363
- CNPJ
- 05638301000169
Company information
- Registration Holder
- TECMEDIC COMÉRCIO DE PRODUTOS MÉDICOS LTDA
- Manufacturer
- AR BALTIC MEDICAL UAB
- Manufacturing Country
- Lithuania
PT: LITUÂNIA
Dates and status
- Publication Date
- Jul 07, 2025
- Validity
- 07/07/2035
- 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 IV medical device is registered under ANVISA number 80202910112 and manufactured by AR BALTIC MEDICAL UAB. The registration is held by TECMEDIC COMÉRCIO DE PRODUTOS MÉDICOS LTDA with validity until Jul 07, 2035.
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