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ANVISA registration 80174300029Valid until Jun 22, 2030

septal occluder

ANVISA Registration Number: 80174300029VALFLUX COMERCIO DE MATERIAIS HOSPITALARES LTDADONGGUAN KEWEI MEDICAL INSTRUMENT CO., LTDRisk Class IV
Verified
Device names
Technical name
septal occluder
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PT: oclusor septal
Commercial name
Oclusores Evermend™ - PDA
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Risk class
Class IV
Registration details
Registration Number
80174300029
Process Number
25351376604202027
CNPJ
03872497000126
Company information
Registration Holder
VALFLUX COMERCIO DE MATERIAIS HOSPITALARES LTDA
Manufacturer
DONGGUAN KEWEI MEDICAL INSTRUMENT CO., LTD
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Jun 22, 2020
Validity
22/06/2030
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for septal occluder in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80174300029 and manufactured by DONGGUAN KEWEI MEDICAL INSTRUMENT CO., LTD. The registration is held by VALFLUX COMERCIO DE MATERIAIS HOSPITALARES LTDA with validity until Jun 22, 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.