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"Kehira" dental implant system - Taiwan Registration 62f3873092db078aa4267eaf5e4efdc0

Access comprehensive regulatory information for "Kehira" dental implant system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 62f3873092db078aa4267eaf5e4efdc0 and manufactured by KYOCERA Medical Corporation Shiga Gamo Plant. The authorized representative in Taiwan is AYERS MEDICAL TRADING CORP..

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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62f3873092db078aa4267eaf5e4efdc0
Registration Details
Taiwan FDA Registration: 62f3873092db078aa4267eaf5e4efdc0
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Device Details

"Kehira" dental implant system
TW: โ€œๅ…‹ๅธŒๆ‹‰โ€ๆค็‰™็ณป็ตฑ
Risk Class 3
Cancelled

Registration Details

62f3873092db078aa4267eaf5e4efdc0

DHA00601917701

Company Information

Product Details

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

F Dentistry

F.3640 Bone Implants

import

Dates and Status

Jun 13, 2009

Aug 27, 2018

Jun 16, 2022

Cancellation Information

Logged out

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