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"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.

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9b4c53ea7f8fa518251f6e5db1f4a68f
Registration Details
Taiwan FDA Registration: 9b4c53ea7f8fa518251f6e5db1f4a68f
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Device Details

"Ivoclar Vivadent" Abrasive device and accessories (Non-Sterile)
TW: "็พฉ็ฒๅ˜‰ๅ‰็“ฆ็™ป็‰น" ็ ”็ฃจ่ฃ็ฝฎๅŠๅ…ถ้™„ไปถ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

9b4c53ea7f8fa518251f6e5db1f4a68f

Ministry of Health Medical Device Import Registration No. 016380

DHA08401638000

Company Information

Liechtenstein

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

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