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Diaswiss Abrasive device and accessories (Non-sterile) - Taiwan Registration a2e829a8d502078d6f9eeda4756100eb

Access comprehensive regulatory information for Diaswiss 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 a2e829a8d502078d6f9eeda4756100eb and manufactured by DIASWISS S. A. The authorized representative in Taiwan is HENG ZUAN TRADE CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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a2e829a8d502078d6f9eeda4756100eb
Registration Details
Taiwan FDA Registration: a2e829a8d502078d6f9eeda4756100eb
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Device Details

Diaswiss Abrasive device and accessories (Non-sterile)
TW: ่ฟช็‘žๅฃซ ็ ”็ฃจ่ฃ็ฝฎๅŠๅ…ถ้™„ไปถ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

a2e829a8d502078d6f9eeda4756100eb

Ministry of Health Medical Device Import Registration No. a00122

DHA084a0012201

Company Information

Switzerland

Product Details

Limited to the first level identification range of grinding devices and their accessories (F.6010) of the classification and grading management methods for medical equipment.

F Dentistry

F6010 Grinding device and accessories

Dates and Status

Oct 12, 2022

Oct 31, 2023