Taiwan FDA registration 8d7ed8c55be3c026722d613d9b4ea4dc

“Coloplast” Ostomy pouch and Accessories (Non-Sterile)

TW: “康樂保”造口術用袋及其附件 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·COLOPLAST (CHINA) LTD.·Registered May 10, 2019 – May 10, 2024Expired
Registration details
Analysis ID
8d7ed8c55be3c026722d613d9b4ea4dc
License Form
Ministry of Health Medical Device Land Transport No. 003790
Customs Code
DHA09600379007
Company information
Manufacturer Country
China
Authorized Representative
COLOPLAST TAIWAN CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Ostomy Bag and Its Accessories (H.5900)".
Product Type (Level 1)
H Gastroenterology-urology devices
Product Type (Level 2)
H5900 Ostomy bag and accessories
Import Information
Imported from abroad; Made in China
Dates and status
Registration Date
May 10, 2019
Expiry Date
May 10, 2024
About this record

Access comprehensive regulatory information for “Coloplast” Ostomy pouch and Accessories (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 8d7ed8c55be3c026722d613d9b4ea4dc and manufactured by COLOPLAST (CHINA) LTD.. The authorized representative in Taiwan is COLOPLAST TAIWAN 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