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"YIKA" Cushion (Non-Sterile) - Taiwan Registration 40e72edfeffd53f68cdfea0ef6097d2c

Access comprehensive regulatory information for "YIKA" 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 40e72edfeffd53f68cdfea0ef6097d2c and manufactured by YIKA MEDICAL CO., LTD.. The authorized representative in Taiwan is YIKA 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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40e72edfeffd53f68cdfea0ef6097d2c
Registration Details
Taiwan FDA Registration: 40e72edfeffd53f68cdfea0ef6097d2c
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Device Details

"YIKA" Cushion (Non-Sterile)
TW: "ๅฎœๅบท" ๆธ›ๅฃ“ๅๅขŠ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

40e72edfeffd53f68cdfea0ef6097d2c

Ministry of Health Medical Device Manufacturing No. 008624

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

Oct 05, 2020

Oct 05, 2025