ANVISA registration

Oclusor PDA Evermend

Registration 81667100083. oclusor septal

Registration details

Registration number81667100083
Application number25351187723202511
Technical nameoclusor septal
Risk classIV
Published on10/08/2026
ValidityValid until 10/08/2036

Registration holder

Legal nameMICROPORT SCIENTIFIC VASCULAR BRASIL LTDA
CNPJ29.182.018/0001-33

Manufacturer

  • DONGGUAN KEWEI MEDICAL INSTRUMENT CO. LTD. CHINA, REPÚBLICA POPULAR

Source: ANVISA

Source: ANVISA open data, medical device file, updated daily. The public database provides registration validity, rather than registration status: this registration may have been cancelled before its expiry date without this being shown here. Before making purchasing, import or marketing decisions, check the ANVISA search portal.

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