"Ivoclar Vivadent" Abrasive device and accessories (Non-Sterile) - Taiwan Registration 9b4c53ea7f8fa518251f6e5db1f4a68f
Access comprehensive regulatory information for "Ivoclar Vivadent" Abrasive device and accessories (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9b4c53ea7f8fa518251f6e5db1f4a68f and manufactured by IVOCLAR VIVADENT AG. The authorized representative in Taiwan is BioLaden Consultant Corp..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including IVOCLAR VIVADENT AG, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Registration Details
9b4c53ea7f8fa518251f6e5db1f4a68f
Ministry of Health Medical Device Import Registration No. 016380
DHA08401638000
Product Details
Limited to the first level identification range of grinding devices and their accessories (F.6010) under the management measures for medical equipment.
F Dental devices
F6010 Grinding device and accessories
Imported from abroad
Dates and Status
Oct 01, 2021
Oct 31, 2026

