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"JOIMAX" Spinal Endoscopic Instruments (Non-Sterile) - Taiwan Registration 17df41129bd5c8babeed2099f8816dd0

Access comprehensive regulatory information for "JOIMAX" Spinal Endoscopic Instruments (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 17df41129bd5c8babeed2099f8816dd0 and manufactured by JOIMAX GMBH. The authorized representative in Taiwan is K&C MEDICAL 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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17df41129bd5c8babeed2099f8816dd0
Registration Details
Taiwan FDA Registration: 17df41129bd5c8babeed2099f8816dd0
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Device Details

"JOIMAX" Spinal Endoscopic Instruments (Non-Sterile)
TW: "่„Š็พŽ้ฉ" ่„ŠๆคŽๅ…ง่ฆ–้กๅทฅๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

17df41129bd5c8babeed2099f8816dd0

Ministry of Health Medical Device Import No. 015192

DHA09401519200

Company Information

Germany

Product Details

Limited to the first level identification range of "Arthroscopy (N.1100)" of the Measures for the Administration of Medical Equipment.

N Orthopedic devices

N1100 Arthroscopy

Imported from abroad

Dates and Status

May 05, 2015

May 05, 2025