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“KJ” Narrow Body Screw System - Taiwan Registration 7d388ea077932db97ce35b0e6a501e4e

Access comprehensive regulatory information for “KJ” Narrow Body Screw System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 7d388ea077932db97ce35b0e6a501e4e and manufactured by KJ MEDITECH CO., LTD.. The authorized representative in Taiwan is Jinpin Technology 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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7d388ea077932db97ce35b0e6a501e4e
Registration Details
Taiwan FDA Registration: 7d388ea077932db97ce35b0e6a501e4e
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Device Details

“KJ” Narrow Body Screw System
TW: “可捷”窄體人工牙根
Risk Class 3
MD

Registration Details

7d388ea077932db97ce35b0e6a501e4e

Department of Health Medical Device Import No. 023017

DHA00602301704

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

Nov 21, 2011

Nov 21, 2026