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

Dental Impression Material - ANVISA Registration 80196880379

Access comprehensive regulatory information for Dental Impression Material in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80196880379 and manufactured by DENTSPLY CAULK. The registration is held by DENTSPLY IND.COM. LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including VIGODENT INDUSTRIA E COMERCIO LTDA., 3M DEUTSCHLAND GMBH, 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
80196880379
Registration Details
ANVISA Registration Number: 80196880379
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Aquasil Ultra+ Smart Wetting
Risk Class I

Registration Details

80196880379

25351841301201874

31116239000155

Company Information

DENTSPLY CAULK
United States of America
PT: ESTADOS UNIDOS DA AMร‰RICA

Dates and Status

Mar 18, 2019

VIGENTE

09/18/2025 19:00:01