ENDOPROSTHESIS (VASCULAR) - ANVISA Registration 81398250022

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 81398250022 and manufactured by JOTEC GMBH. The registration is held by Jotec do Brasil importação e comercio de equipamentos hospitalares ltda with validity until Jun 16, 2035.

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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81398250022
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Registration Details
ANVISA Registration Number: 81398250022
Janaina dos Santos de Miranda

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Related Devices (2)

E-vita® OPEN NEO
Risk Class IV

Registration Details

81398250022

25351854179202363

21996505000128

Company Information

JOTEC GMBH
Germany
PT: ALEMANHA

Dates and Status

Jun 16, 2025

16/06/2035

09/18/2025 19:00:01

E-vita® OPEN NEO
Risk Class IV

Registration Details

81398250022

25351854179202363

21996505000128

Dates and Status

Jun 16, 2025

16/06/2035

09/18/2025 19:00:01