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“Joson Care”Plinth (Non-Sterile) - Taiwan Registration 883cfa84a0757a71492e7d7c583f9bfe

Access comprehensive regulatory information for “Joson Care”Plinth (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 883cfa84a0757a71492e7d7c583f9bfe and manufactured by Qiangshengxing Enterprise Co., Ltd. Guishan Factory. The authorized representative in Taiwan is Qiangshengxing Enterprise Co., Ltd. Guishan Factory.

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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883cfa84a0757a71492e7d7c583f9bfe
Registration Details
Taiwan FDA Registration: 883cfa84a0757a71492e7d7c583f9bfe
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Device Details

“Joson Care”Plinth (Non-Sterile)
TW: “強盛興”治療檯(未滅菌)
Risk Class 1
MD

Registration Details

883cfa84a0757a71492e7d7c583f9bfe

Ministry of Health Medical Device Manufacturing Registration No. 004679

Company Information

Product Details

Limited to the first-level identification range of the Measures for the Administration of Medical Equipment "Treatment Table (O.3520)".

o Equipment for physical medicine

O3520 treatment unit

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2023