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ANVISA registration 80312270079Valid until Mar 21, 2036

CORONARY ANGIOPLASTY BALLOON CATHETER

ANVISA Registration Number: 80312270079TELEFLEX MEDICAL BRASIL LTDABIOTRONIK AGRisk Class IV
Verified
Device names
Technical name
CORONARY ANGIOPLASTY BALLOON CATHETER
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PT: CATETER BALÃO PARA ANGIOPLASTIA CORONÁRIA
Commercial name
CATETER DE DILATAÇÃO CORONÁRIA PANTERA PRO
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Risk class
Class IV
Registration details
Registration Number
80312270079
Process Number
25351175225202526
CNPJ
06089071000199
Company information
Registration Holder
TELEFLEX MEDICAL BRASIL LTDA
Manufacturer
BIOTRONIK AG
Manufacturing Country
Switzerland
PT: SUÍÇA
Dates and status
Publication Date
Oct 24, 2025
Validity
21/03/2036
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 80312270079 and manufactured by BIOTRONIK AG. The registration is held by TELEFLEX MEDICAL BRASIL LTDA with validity until Mar 21, 2036.

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.