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ANVISA registration 10407990082Valid until Jan 06, 2030

CORONARY ANGIOPLASTY BALLOON CATHETER

ANVISA Registration Number: 10407990082ANGIOMED IMPORTACAO E EXPORTACAO LTDASimeks Tibbi Urunler Sanayi ve Ticaret Limited SirketiRisk Class IV
Verified
Device names
Technical name
CORONARY ANGIOPLASTY BALLOON CATHETER
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PT: CATETER BALÃO PARA ANGIOPLASTIA CORONÁRIA
Commercial name
Simpass HP-NC RX Cateter Balão para PTCA
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Risk class
Class IV
Registration details
Registration Number
10407990082
Process Number
25351533284201985
CNPJ
02699256000164
Company information
Registration Holder
ANGIOMED IMPORTACAO E EXPORTACAO LTDA
Manufacturer
Simeks Tibbi Urunler Sanayi ve Ticaret Limited Sirketi
Manufacturing Country
Türkiye
PT: TURQUIA
Dates and status
Publication Date
Jan 06, 2020
Validity
06/01/2030
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 10407990082 and manufactured by Simeks Tibbi Urunler Sanayi ve Ticaret Limited Sirketi. The registration is held by ANGIOMED IMPORTACAO E EXPORTACAO LTDA with validity until Jan 06, 2030.

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.