Taiwan FDA registration b4a66d09890e2c5218ac24d24f5ff964

Shengda antipyretic patch (unsterilized) 

TW: “生達”退熱貼 (未滅菌) 
Taiwan flagTaiwan·Risk Class 1·DIA PHARMACEUTICAL CO., LTD.·Registered Nov 22, 2010 – Nov 22, 2025Cancelled
Registration details
Analysis ID
b4a66d09890e2c5218ac24d24f5ff964
Customs Code
DHA04400956001
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 Physical Medical Sciences
Product Type (Level 2)
O.5700 醫療用冷熱敷裝置
Import Information
import
Dates and status
Registration Date
Nov 22, 2010
Expiry Date
Nov 22, 2025
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
About this record

Access comprehensive regulatory information for Shengda antipyretic patch (unsterilized)  in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b4a66d09890e2c5218ac24d24f5ff964 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