optical fiber - ANVISA Registration 81521800004

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 81521800004 and manufactured by G.N.S. NEOLASER LTD.. The registration is held by BPF MEDICAL DISTRIBUIDORA E IMPORTADORA DE PRODUTOS MEDICOS LTDA-ME with validity until Jul 29, 2029.

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, 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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81521800004
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Registration Details
ANVISA Registration Number: 81521800004
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Probe NeoV Corona Fístula
Risk Class III

Registration Details

81521800004

25351228563202225

27622775000155

Company Information

Israel
PT: ISRAEL

Dates and Status

Apr 18, 2022

29/07/2029

09/18/2025 19:00:01

Probe NeoV Corona Fístula
Risk Class III

Registration Details

81521800004

25351228563202225

27622775000155

Dates and Status

Apr 18, 2022

29/07/2029

09/18/2025 19:00:01