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ANVISA registration 10407990053Active

PERIPHERAL ANGIOPLASTY BALLOON CATHETER

ANVISA Registration Number: 10407990053ANGIOMED IMPORTACAO E EXPORTACAO LTDASimeks Tibbi Urunler Sanayi ve Ticaret Limited SirketiRisk Class II
Verified
Device names
Technical name
PERIPHERAL ANGIOPLASTY BALLOON CATHETER
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PT: CATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA
Commercial name
Simpass Endo 35 OTW- Cateter balão para PTA
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Risk class
Class II
Registration details
Registration Number
10407990053
Process Number
25351039678201705
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
Feb 13, 2017
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 10407990053 and manufactured by Simeks Tibbi Urunler Sanayi ve Ticaret Limited Sirketi. The registration is held by ANGIOMED IMPORTACAO E EXPORTACAO LTDA with validity until currently active (VIGENTE).

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.