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ANVISA registration 81667100083Valid until Aug 10, 2036

septal occluder

ANVISA Registration Number: 81667100083MICROPORT SCIENTIFIC VASCULAR BRASIL LTDADONGGUAN KEWEI MEDICAL INSTRUMENT CO. LTD.Risk Class IV
Verified
Device names
Technical name
septal occluder
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PT: oclusor septal
Commercial name
Oclusor PDA Evermend
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Risk class
Class IV
Registration details
Registration Number
81667100083
Process Number
25351187723202511
CNPJ
29182018000133
Company information
Registration Holder
MICROPORT SCIENTIFIC VASCULAR BRASIL LTDA
Manufacturer
DONGGUAN KEWEI MEDICAL INSTRUMENT CO. LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Aug 10, 2026
Validity
10/08/2036
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 81667100083 and manufactured by DONGGUAN KEWEI MEDICAL INSTRUMENT CO. LTD.. The registration is held by MICROPORT SCIENTIFIC VASCULAR BRASIL LTDA with validity until Aug 10, 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.