Taiwan FDA registration a424efa0e6ec60c38747bb73e06491b5

“Kenda” Abrasive Device and Accessories (non-sterile)

TW: “肯答”研磨裝置及其附件 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·COLTENE/WHALEDENT AG·Registered Oct 01, 2021 – Oct 31, 2026Active
Registration details
Analysis ID
a424efa0e6ec60c38747bb73e06491b5
License Form
Ministry of Health Medical Device Import Registration No. 022331
Customs Code
DHA08402233109
Company information
Manufacturer Country
Switzerland
Authorized Representative
THREE A CO., LTD.
Product details
Intended Use
Limited to the first level identification range of grinding devices and their accessories (F.6010) under the management measures for medical equipment.
Product Type (Level 1)
F Dental devices
Product Type (Level 2)
F6010 Grinding device and accessories
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2026
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About this record

Access comprehensive regulatory information for “Kenda” 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 a424efa0e6ec60c38747bb73e06491b5 and manufactured by COLTENE/WHALEDENT AG. The authorized representative in Taiwan is THREE A CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including COLTENE/WHALEDENT 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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