ORAL DEVICE FOR REDUCING BITE CAPACITY - ANVISA Registration 80102512173
Access comprehensive regulatory information for ORAL DEVICE FOR REDUCING BITE CAPACITY in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80102512173 and manufactured by AKERVALL TECHNOLOGIES. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS 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 JIANGSU VEDKANG MEDICAL SCIENCE & TECHNOLOGY CO., LTD., DENTRADE GMBH & CO.KG, 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
80102512173
25351500883201751
04718143000194
Company Information
Dates and Status
Feb 18, 2019
VIGENTE
09/18/2025 19:00:01
DISPOSITIVO ORAL PARA REDUÇÃO DA CAPACIDADE DE MORDIDA
Bite Blocks
JIANGSU VEDKANG MEDICAL SCIENCE & TECHNOLOGY CO., LTD.
80102513404
Apr 07, 2025
DISPOSITIVO ORAL PARA REDUÇÃO DA CAPACIDADE DE MORDIDA
RehaSplint®
DENTRADE GMBH & CO.KG
80456680014
Aug 26, 2024

