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“JO” Inter-X Lumbar Fusion Cage - Taiwan Registration ee025d1b0c25bfc765b09cd0a6701f37

Access comprehensive regulatory information for “JO” Inter-X Lumbar Fusion Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ee025d1b0c25bfc765b09cd0a6701f37 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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ee025d1b0c25bfc765b09cd0a6701f37
Registration Details
Taiwan FDA Registration: ee025d1b0c25bfc765b09cd0a6701f37
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Device Details

“JO” Inter-X Lumbar Fusion Cage
TW: “傑奎”穎特司腰椎融合器
Risk Class 2
MD

Registration Details

ee025d1b0c25bfc765b09cd0a6701f37

Ministry of Health Medical Device Manufacturing No. 005447

Company Information

Taiwan, Province of China

Product Details

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

N Orthopedic devices

N3060 Spine correction fixation between vertebral bodies

Produced in Taiwan, China

Dates and Status

Sep 05, 2016

Sep 05, 2026