FIBERGLASS-BASED MATERIAL FOR DENTAL PROSTHESIS MANUFACTURING - ANVISA Registration 80172319028
Access comprehensive regulatory information for FIBERGLASS-BASED MATERIAL FOR DENTAL PROSTHESIS MANUFACTURING in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80172319028 and manufactured by DENTSCARE LTDA. The registration is held by DENTSCARE LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 3 companies making the same product including INTRA-LOCK IND.COM.IMP.EXP.DE PRODS.IMPLANTOLOG, BIOFUNCTIONAL MATERIALS LLC, and 3 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
80172319028
25351049138202514
05106945000106
Company Information
Dates and Status
Apr 28, 2025
VIGENTE
09/18/2025 19:00:01
MATERIAL A BASE DE FIBRA DE VIDRO PARA CONFECÇÃO DE PRÓTESE DENTAL
ZANTEX BR Polímero Reforçado com Fibra de Vidro
INTRA-LOCK IND.COM.IMP.EXP.DE PRODS.IMPLANTOLOG
10352719001
Feb 27, 2023
MATERIAL A BASE DE FIBRA DE VIDRO PARA CONFECÇÃO DE PRÓTESE DENTAL
ZANTEX™ Polímero Reforçado com Fibra de Vidro
BIOFUNCTIONAL MATERIALS LLC
10352710015
Sep 09, 2019
MATERIAL A BASE DE FIBRA DE VIDRO PARA CONFECÇÃO DE PRÓTESE DENTAL
Trilor Fiber
Bioloren S.r.l.
81361440031
Jun 03, 2019

