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“DIO” Protem Implant System - Taiwan Registration a626d5828001b53606ab4f52ee2d0e00

Access comprehensive regulatory information for “DIO” Protem 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 a626d5828001b53606ab4f52ee2d0e00 and manufactured by DIO CORPORATION. The authorized representative in Taiwan is DIO IMPLANT TAIWAN CORPORATION.

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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a626d5828001b53606ab4f52ee2d0e00
Registration Details
Taiwan FDA Registration: a626d5828001b53606ab4f52ee2d0e00
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Device Details

“DIO” Protem Implant System
TW: “帝歐”波登植體系統
Risk Class 3
MD

Registration Details

a626d5828001b53606ab4f52ee2d0e00

Ministry of Health Medical Device Import No. 027636

DHA05602763606

Company Information

Korea, Republic of

Product Details

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

F Dental devices

F3640 Bone explants

Imported from abroad

Dates and Status

Aug 18, 2015

Aug 18, 2025