ANVISA registration 80067930046Valid until Apr 19, 2031ENDOPROSTHESIS (VASCULAR)
ANVISA Registration Number: 80067930046W.L. GORE & ASSOCIATES DO BRASIL LTDA.W.L. GORE & ASSOCIATES, INC (N. FOURTH STREET)Risk Class IV
Device names
- Technical name
- ENDOPROSTHESIS (VASCULAR)
- Commercial name
- GORE® VIABAHN® Endoprosthesis with PROPATEN® Bioactive Surface
- Risk class
- Class IV
PT: ENDOPRÓTESE (VASCULAR)
Registration details
- Registration Number
- 80067930046
- Process Number
- 25351723230202043
- 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
- Apr 19, 2021
- Validity
- 19/04/2031
- 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 80067930046 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 Apr 19, 2031.
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