Physiotherapeutic Vibrating Equipment - ANVISA Registration 80413800004
Access comprehensive regulatory information for Physiotherapeutic Vibrating Equipment in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80413800004 and manufactured by PROMOITALIA GROUP SPA. The registration is held by PHARMEDIC PHARMACEUTICALS IMPORTAÇÃO, DISTRIBUIÇÃO, COMÉRCIO E REPRESENTAÇÕES LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 2 companies making the same product including FOUNTAIN HEAD MARKETING, INC DBA ROMET ELETRONIC LARYNX, K1MED CO., LTD., 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.
Device Details
Registration Details
80413800004
25351621891200849
07453785000105
Company Information
Dates and Status
Apr 05, 2010
VIGENTE
09/18/2025 19:00:01
Equipamento Vibrador Fisioterapêutico
Sistema de Terapia de ondas extracorpórea COMBO WAVE
K1MED CO., LTD.
80380269014
Oct 28, 2021
Equipamento Vibrador Fisioterapêutico
LARINGE ELETRONICA
FOUNTAIN HEAD MARKETING, INC DBA ROMET ELETRONIC LARYNX
80320680008
May 20, 2013

