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ANVISA registration 81778810068Valid until Jun 22, 2036

CORONARY ANGIOPLASTY BALLOON CATHETER

ANVISA Registration Number: 81778810068LATIN HEALTH IMPORTADORA E DISTRIBUIDORA LTDA.BROSMED MEDICAL CO., LTDRisk Class IV
Verified
Device names
Technical name
CORONARY ANGIOPLASTY BALLOON CATHETER
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PT: CATETER BALÃO PARA ANGIOPLASTIA CORONÁRIA
Commercial name
APERI SC Balloon Dilatation Catheter
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Risk class
Class IV
Registration details
Registration Number
81778810068
Process Number
25351089494202571
CNPJ
29986299000187
Company information
Registration Holder
LATIN HEALTH IMPORTADORA E DISTRIBUIDORA LTDA.
Manufacturer
BROSMED MEDICAL CO., LTD
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Jun 22, 2026
Validity
22/06/2036
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 81778810068 and manufactured by BROSMED MEDICAL CO., LTD. The registration is held by LATIN HEALTH IMPORTADORA E DISTRIBUIDORA LTDA. with validity until Jun 22, 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.