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"Ivoclar Vivadent" Abrasive device and accessories (Non-Sterile) - Taiwan Registration d6a9534ed2760e762175f5fafbc9f474

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 d6a9534ed2760e762175f5fafbc9f474 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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d6a9534ed2760e762175f5fafbc9f474
Registration Details
Taiwan FDA Registration: d6a9534ed2760e762175f5fafbc9f474
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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
Cancelled

Registration Details

d6a9534ed2760e762175f5fafbc9f474

Ministry of Health Medical Device Import No. 016380

DHA09401638006

Company Information

Liechtenstein

Product Details

F Dental devices

F6010 Grinding device and accessories

Imported from abroad

Dates and Status

Apr 12, 2016

Apr 12, 2026

Cancellation Information

Logged out

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