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ANVISA registration 81667100050Valid until Jul 04, 2032

PERIPHERAL ANGIOPLASTY BALLOON CATHETER

ANVISA Registration Number: 81667100050MICROPORT SCIENTIFIC VASCULAR BRASIL LTDASHANGHAI MICROPORT ENDOVASCULAR MEDTECH (GROUP) CO., LTD.Risk Class IV
Verified
Device names
Technical name
PERIPHERAL ANGIOPLASTY BALLOON CATHETER
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PT: CATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA
Commercial name
Reewarm PTX Cateter Balão PTA revestido com fármaco
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Risk class
Class IV
Registration details
Registration Number
81667100050
Process Number
25351090069202109
CNPJ
29182018000133
Company information
Registration Holder
MICROPORT SCIENTIFIC VASCULAR BRASIL LTDA
Manufacturer
SHANGHAI MICROPORT ENDOVASCULAR MEDTECH (GROUP) CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Jul 04, 2022
Validity
04/07/2032
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 81667100050 and manufactured by SHANGHAI MICROPORT ENDOVASCULAR MEDTECH (GROUP) CO., LTD.. The registration is held by MICROPORT SCIENTIFIC VASCULAR BRASIL LTDA with validity until Jul 04, 2032.

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.