Physiotherapeutic Vibrating Equipment - ANVISA Registration 80320680008
Access comprehensive regulatory information for Physiotherapeutic Vibrating Equipment in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80320680008 and manufactured by FOUNTAIN HEAD MARKETING, INC DBA ROMET ELETRONIC LARYNX. The registration is held by DANIALEX TEC - MATERIAL MEDICO HOSPITALAR LTDA ME with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 2 companies making the same product including K1MED CO., LTD., PROMOITALIA GROUP SPA, and 2 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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Registration Details
80320680008
25351215593201344
01686305000161
Company Information
Dates and Status
May 20, 2013
VIGENTE
09/18/2025 19:00:01
Physiotherapeutic Vibrating Equipment
PROELLIXE VIBRATION
PROMOITALIA GROUP SPA
80413800004
Apr 05, 2010
Physiotherapeutic Vibrating Equipment
Sistema de Terapia de ondas extracorpórea COMBO WAVE
K1MED CO., LTD.
80380269014
Oct 28, 2021
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80244300005
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Sistema de Terapia de ondas extracorpórea COMBO WAVE
K1MED CO., LTD.
80380269014
Oct 28, 2021
Equipamento Vibrador Fisioterapêutico
PROELLIXE VIBRATION
PROMOITALIA GROUP SPA
80413800004
Apr 05, 2010