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optical fiber - ANVISA Registration 80444810102

Access comprehensive regulatory information for optical fiber in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80444810102 and manufactured by TEDAN SURGICAL INNOVATIONS INC. The registration is held by HIGHRIDGE MEDICAL BRASIL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME, LUMENIS 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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80444810102
Registration Details
ANVISA Registration Number: 80444810102
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Device Details

CABO DE LUZ PHANTOM ML REUTILIZAVEL
Risk Class I

Registration Details

80444810102

25351620226202377

08954683000128

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Oct 16, 2023

VIGENTE

09/18/2025 19:00:01