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optical fiber - ANVISA Registration 10383700068

Access comprehensive regulatory information for optical fiber in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10383700068 and manufactured by VK DRILLER EQUIPAMENTOS ELÉTRICOS LTDA. The registration is held by VK DRILLER EQUIPAMENTOS ELÉTRICOS LTDA with validity until Mar 14, 2032.

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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10383700068
Registration Details
ANVISA Registration Number: 10383700068
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Device Details

FIBRA ÓPTICA DIOLUX ENDOLUMINAL
Risk Class III

Registration Details

10383700068

25351093601202212

68996560000181

Company Information

Brazil
PT: BRASIL

Dates and Status

Mar 14, 2022

14/03/2032

09/18/2025 19:00:01