Pure Global AI
ANVISA registration 80067930051Valid until May 11, 2036

INTRAVASCULAR GUIDE CATHETER

ANVISA Registration Number: 80067930051W.L. GORE & ASSOCIATES DO BRASIL LTDA.W.L. GORE & ASSOCIATES, INC..Risk Class IV
Verified
Device names
Technical name
INTRAVASCULAR GUIDE CATHETER
View exact technical-name matches →
PT: CATETER GUIA INTRAVASCULAR
Commercial name
GORE® Tri-Lumen Catheter (TLC®)
View exact commercial-name matches →
Risk class
Class IV
Registration details
Registration Number
80067930051
Process Number
25351121624202577
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
May 11, 2026
Validity
11/05/2036
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for INTRAVASCULAR GUIDE CATHETER in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80067930051 and manufactured by W.L. GORE & ASSOCIATES, INC... The registration is held by W.L. GORE & ASSOCIATES DO BRASIL LTDA. with validity until May 11, 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.