ENDOPROSTHESIS (VASCULAR) - ANVISA Registration 81398250001

Access comprehensive regulatory information for ENDOPROSTHESIS (VASCULAR) in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81398250001 and manufactured by manufacturer not specified. The registration is held by Jotec do Brasil importação e comercio de equipamentos hospitalares ltda with validity until Jun 06, 2026.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including BOSTON SCIENTIFIC CORPORATION - MARLBOROUGH, LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD., 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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81398250001
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Registration Details
ANVISA Registration Number: 81398250001
Janaina dos Santos de Miranda

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Related Devices (2)

Stent Periférico Recoberto E-ventus BX
Risk Class III

Registration Details

81398250001

25351112239201991

21996505000128

Dates and Status

Apr 01, 2019

06/06/2026

09/18/2025 19:00:01

Stent Periférico Recoberto E-ventus BX
Risk Class III

Registration Details

81398250001

25351112239201991

21996505000128

Company Information

JOTEC GMBH
Germany
PT: ALEMANHA

Dates and Status

Apr 01, 2019

06/06/2026

09/18/2025 19:00:01