Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

optical fiber - ANVISA Registration 80603600106

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 80603600106 and manufactured by HUMMER DO BRASIL COMERCIAL IMP E EXP. DE EQUIPS HOSPITALARES LTDA. The registration is held by HUMMER DO BRASIL COMERCIAL IMP E EXP. DE EQUIPS HOSPITALARES LTDA with validity until Nov 04, 2029.

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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
80603600106
Registration Details
ANVISA Registration Number: 80603600106
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

FIBRA LASER REUTILIZÁVEL
Risk Class III

Registration Details

80603600106

25351160923201989

09553187000125

Company Information

Dates and Status

Nov 04, 2019

04/11/2029

09/18/2025 19:00:01