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ANVISA registration 80067930041Valid until Nov 18, 2029

septal occluder

ANVISA Registration Number: 80067930041W.L. GORE & ASSOCIATES DO BRASIL LTDA.W.L. GORE & ASSOCIATES, INCRisk Class IV
Verified
Device names
Technical name
septal occluder
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PT: oclusor septal
Commercial name
GORE® CARDIOFORM SEPTAL OCCLUDER
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Risk class
Class IV
Registration details
Registration Number
80067930041
Process Number
25351454389201979
CNPJ
03806796000162
Company information
Registration Holder
W.L. GORE & ASSOCIATES DO BRASIL LTDA.
Manufacturer
W.L. GORE & ASSOCIATES, INC
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Nov 18, 2019
Validity
18/11/2029
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 80067930041 and manufactured by W.L. GORE & ASSOCIATES, INC. The registration is held by W.L. GORE & ASSOCIATES DO BRASIL LTDA. with validity until Nov 18, 2029.

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.