ANVISA registration 80067930052Valid until May 25, 2036ENDOPROSTHESIS (VASCULAR)
ANVISA Registration Number: 80067930052W.L. GORE & ASSOCIATES DO BRASIL LTDA.W.L. GORE & ASSOCIATES, INC..Risk Class IV
Device names
- Technical name
- ENDOPROSTHESIS (VASCULAR)
- Commercial name
- GORE® PROPATEN® Vascular Graft Configured for Pediatric Shunt
- Risk class
- Class IV
PT: ENDOPRÓTESE (VASCULAR)
Registration details
- Registration Number
- 80067930052
- Process Number
- 25351198136202558
- 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 25, 2026
- Validity
- 25/05/2036
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for ENDOPROSTHESIS (VASCULAR) in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80067930052 and manufactured by W.L. GORE & ASSOCIATES, INC... The registration is held by W.L. GORE & ASSOCIATES DO BRASIL LTDA. with validity until May 25, 2036.
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