Fiber optic cables/bundles - ANVISA Registration 80102513490

Access comprehensive regulatory information for Fiber optic cables/bundles in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80102513490 and manufactured by DORNIER MEDTECH AMERICA. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Aug 04, 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 E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME, DORNIER MEDTECH AMERICA, 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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80102513490
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Registration Details
ANVISA Registration Number: 80102513490
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Cânula de Fibra Laser de Uso Único Dornier
Risk Class III

Registration Details

80102513490

25351084437202503

04718143000194

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Aug 04, 2025

04/08/2035

09/18/2025 19:00:01

Cânula de Fibra Laser de Uso Único Dornier
Risk Class III

Registration Details

80102513490

25351084437202503

04718143000194

Dates and Status

Aug 04, 2025

04/08/2035

09/18/2025 19:00:01