Taiwan FDA registration 25408aae6f09e68316f2640ddd819b4e

“Standard”Genki Cooling Gel Sheet (Non-Sterile) 

TW: “生達”退熱貼 (未滅菌) 
Taiwan flagTaiwan·Risk Class 1·MD·DIA PHARMACEUTICAL CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2026Active
Registration details
Analysis ID
25408aae6f09e68316f2640ddd819b4e
License Form
Ministry of Health Medical Device Import Registration No. 009560
Customs Code
DHA08400956008
Company information
Manufacturer Country
Japan
Authorized Representative
STANDARD CHEM. & PHARM. CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Medical Cold Compress Pack (O.5700)".
Product Type (Level 1)
o Equipment for physical medicine
Product Type (Level 2)
O5700 Medical Cold Pack
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2026
About this record

Access comprehensive regulatory information for “Standard”Genki Cooling Gel Sheet (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 25408aae6f09e68316f2640ddd819b4e and manufactured by DIA PHARMACEUTICAL CO., LTD.. The authorized representative in Taiwan is STANDARD CHEM. & PHARM. 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.

Free DatabasePowered by Pure Global AI89,000+ Devices