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“JO” PCF Posterior Cervical Fixation System - Taiwan Registration 3ae5452dab94f4afbc2b29540ba9acca

Access comprehensive regulatory information for “JO” PCF Posterior Cervical Fixation System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3ae5452dab94f4afbc2b29540ba9acca and manufactured by Jiekui Technology Co., Ltd. Nanke Branch. The authorized representative in Taiwan is Jiekui Technology Co., Ltd. Nanke Branch.

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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3ae5452dab94f4afbc2b29540ba9acca
Registration Details
Taiwan FDA Registration: 3ae5452dab94f4afbc2b29540ba9acca
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Device Details

“JO” PCF Posterior Cervical Fixation System
TW: “傑奎”比希弗頸椎後方固定系統
Risk Class 3
MD

Registration Details

3ae5452dab94f4afbc2b29540ba9acca

Ministry of Health Medical Device Manufacturing No. 005453

Company Information

Taiwan, Province of China

Product Details

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

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N3070 Pedicle screw system

Produced in Taiwan, China

Dates and Status

Sep 22, 2016

Sep 22, 2026