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"Kejie" narrow body artificial tooth root - Taiwan Registration 781fbdde7e7b47ce0ee57d03c2e3c27c

Access comprehensive regulatory information for "Kejie" narrow body artificial tooth root in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 781fbdde7e7b47ce0ee57d03c2e3c27c and manufactured by KJ MEDITECH CO., LTD.. The authorized representative in Taiwan is FUGINGTONE CO..

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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781fbdde7e7b47ce0ee57d03c2e3c27c
Registration Details
Taiwan FDA Registration: 781fbdde7e7b47ce0ee57d03c2e3c27c
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Device Details

"Kejie" narrow body artificial tooth root
TW: โ€œๅฏๆทโ€็ช„้ซ”ไบบๅทฅ็‰™ๆ น
Risk Class 3

Registration Details

781fbdde7e7b47ce0ee57d03c2e3c27c

DHA00602301704

Company Information

Korea, Republic of

Product Details

For details, it is Chinese approved copy of the imitation order

F Dentistry

F.3640 Bone Implants

import

Dates and Status

Nov 21, 2011

Nov 21, 2026