Taiwan FDA registration 40e72edfeffd53f68cdfea0ef6097d2c

"YIKA" Cushion (Non-Sterile)

TW: "宜康" 減壓坐墊 (未滅菌)

Taiwan·Risk Class 1·MD·YIKA MEDICAL CO., LTD.·Registered Oct 05, 2020 – Oct 05, 2025Expired

Registration details

Analysis ID: 40e72edfeffd53f68cdfea0ef6097d2c
License Form: Ministry of Health Medical Device Manufacturing No. 008624

Company information

Manufacturer: YIKA MEDICAL CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: YIKA MEDICAL CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Floating Cushion (O.3175)".
Product Type (Level 1): o Equipment for physical medicine
Product Type (Level 2): O3175 floating seat cushion
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Oct 05, 2020
Expiry Date: Oct 05, 2025

About this record

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.