Fiber optic cables/bundles - ANVISA Registration 80179630004

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 80179630004 and manufactured by manufacturer not specified. The registration is held by HIGHLAS DO BRASIL LTDA with validity until Mar 21, 2036.

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 DORNIER MEDTECH AMERICA, E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME, 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Similar Products
5 Competitors
80179630004
2 Related Devices
Registration Details
ANVISA Registration Number: 80179630004
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Related Devices (2)

FIBRA ENDOLUMINAL ORLIGHT FIBER
Risk Class III

Registration Details

80179630004

25351328048201028

05208227000140

Company Information

Dates and Status

Mar 21, 2011

21/03/2036

09/18/2025 19:00:01

FIBRA ENDOLUMINAL ORLIGHT FIBER
Risk Class III

Registration Details

80179630004

25351328048201028

05208227000140

Company Information

MEGABAY S.A
Argentina
PT: ARGENTINA

Dates and Status

Mar 21, 2011

21/03/2036

09/18/2025 19:00:01