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“joimax” Shrill System - Taiwan Registration 1980ff1c45795a0d2b39832992c6547e

Access comprehensive regulatory information for “joimax” Shrill System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1980ff1c45795a0d2b39832992c6547e 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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1980ff1c45795a0d2b39832992c6547e
Registration Details
Taiwan FDA Registration: 1980ff1c45795a0d2b39832992c6547e
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Device Details

“joimax” Shrill System
TW: “傑醫”希爾刨削系統
Risk Class 2
MD

Registration Details

1980ff1c45795a0d2b39832992c6547e

Ministry of Health Medical Device Import No. 032508

DHA05603250804

Company Information

Germany

Product Details

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

N Orthopedic devices

N1100 Arthroscopy

Imported from abroad

Dates and Status

Apr 15, 2019

Apr 15, 2024