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ANVISA registration 80067930043Valid until May 25, 2030

septal occluder

ANVISA Registration Number: 80067930043W.L. GORE & ASSOCIATES DO BRASIL LTDA.W.L. GORE & ASSOCIATES, INC (N. FOURTH STREET)Risk Class IV
Verified
Device names
Technical name
septal occluder
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PT: oclusor septal
Commercial name
GORE® CARDIOFORM ASD Occluder
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Risk class
Class IV
Registration details
Registration Number
80067930043
Process Number
25351148797202028
CNPJ
03806796000162
Company information
Registration Holder
W.L. GORE & ASSOCIATES DO BRASIL LTDA.
Manufacturer
W.L. GORE & ASSOCIATES, INC (N. FOURTH STREET)
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
May 25, 2020
Validity
25/05/2030
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 80067930043 and manufactured by W.L. GORE & ASSOCIATES, INC (N. FOURTH STREET). The registration is held by W.L. GORE & ASSOCIATES DO BRASIL LTDA. with validity until May 25, 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.