Surgical Equipment for Discectomy - ANVISA Registration 80071910122

Access comprehensive regulatory information for Surgical Equipment for Discectomy in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80071910122 and manufactured by OSTEOMED S.A. The registration is held by OSTEOMED S.A with validity until Oct 29, 2034.

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including MARDEN MEDICAL LTDA, SEAWON MEDITECH 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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80071910122
Registration Details
ANVISA Registration Number: 80071910122
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

Kit Cânula Bipolar para Endoscopia Vert-FLEX
Risk Class IV

Registration Details

80071910122

25351394955202443

00638390000120

Company Information

OSTEOMED S.A
Brazil
PT: BRASIL

Dates and Status

Oct 29, 2024

29/10/2034

09/18/2025 19:00:01