Taiwan FDA registration d84f059c1a213e6e5f4ddbf7309276a8
“Coloplast” SenSura Ostomy Pouch and Accessories (Non-Sterile)
TW: “康樂保” 善舒樂造口術用袋及其附件 (未滅菌)
Registration details
- Analysis ID
- d84f059c1a213e6e5f4ddbf7309276a8
- License Form
- Ministry of Health Medical Device Import No. 022724
- Customs Code
- DHA09402272401
Company information
- Manufacturer
- COLOPLAST VOLUME MFG. COSTA RICA SA
- Manufacturer Country
- Costa Rica
- Authorized Representative
- COLOPLAST TAIWAN CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "ostomy bag and its accessories (H.5900)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H5900 Ostomy bag and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 11, 2022
- Expiry Date
- Jan 11, 2027
About this record
Access comprehensive regulatory information for “Coloplast” SenSura 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 d84f059c1a213e6e5f4ddbf7309276a8 and manufactured by COLOPLAST VOLUME MFG. COSTA RICA SA. 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