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“ROODINSEAT” Cube Gel Cushion(Non-Sterile) - Taiwan Registration 9f2937d157e5ed19a0616670e598114e

Access comprehensive regulatory information for “ROODINSEAT” Cube Gel Cushion(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 9f2937d157e5ed19a0616670e598114e and manufactured by ROODINSEAT CORPORATION. The authorized representative in Taiwan is ROODINSEAT CORPORATION.

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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9f2937d157e5ed19a0616670e598114e
Registration Details
Taiwan FDA Registration: 9f2937d157e5ed19a0616670e598114e
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Device Details

“ROODINSEAT” Cube Gel Cushion(Non-Sterile)
TW: “鑫成” 液態凝膠座墊(未滅菌)
Risk Class 1
MD

Registration Details

9f2937d157e5ed19a0616670e598114e

Ministry of Health Medical Device Manufacturing No. 008103

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Floating Cushion (O.3175)".

o Equipment for physical medicine

O3175 floating seat cushion

Produced in Taiwan, China

Dates and Status

Dec 24, 2019

Dec 24, 2024