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Vascular Endoprosthesis - ANVISA Registration 80067930040

Access comprehensive regulatory information for Vascular Endoprosthesis in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80067930040 and manufactured by manufacturer not specified. The registration is held by W.L. GORE & ASSOCIATES DO BRASIL LTDA. with validity until Aug 26, 2029.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including BENTLEY INNOMED GMBH, BOLTON MEDICAL, INC., and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

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80067930040
2 Related Devices
Registration Details
ANVISA Registration Number: 80067930040
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Related Devices (2)

GORE® EXCLUDER® ILIAC BRANCH ENDOPROSTHESIS
Risk Class III

Registration Details

80067930040

25351138842201907

03806796000162

Company Information

Dates and Status

Aug 26, 2019

26/08/2029

09/18/2025 19:00:01

GORE® EXCLUDER® ILIAC BRANCH ENDOPROSTHESIS
Risk Class III

Registration Details

80067930040

25351138842201907

03806796000162

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Aug 26, 2019

26/08/2029

09/18/2025 19:00:01