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ANVISA registration 80202910070Valid until Apr 22, 2034

septal occluder

ANVISA Registration Number: 80202910070TECMEDIC COMÉRCIO DE PRODUTOS MÉDICOS LTDAOCCLUTECH GMBHRisk Class IV
Verified
Device names
Technical name
septal occluder
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PT: oclusor septal
Commercial name
FIGULLA FLEX II PFO
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Risk class
Class IV
Registration details
Registration Number
80202910070
Process Number
25351188508201372
CNPJ
05638301000169
Company information
Registration Holder
TECMEDIC COMÉRCIO DE PRODUTOS MÉDICOS LTDA
Manufacturer
OCCLUTECH GMBH
Manufacturing Country
Germany
PT: ALEMANHA
Dates and status
Publication Date
Apr 22, 2014
Validity
22/04/2034
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 80202910070 and manufactured by OCCLUTECH GMBH. The registration is held by TECMEDIC COMÉRCIO DE PRODUTOS MÉDICOS LTDA with validity until Apr 22, 2034.

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.