Taiwan FDA registration fd89589b440e78d1413a172428df4f69
"Coloplast" Extra Large Urostomy Pocket
TW: "康樂保" 愛特大泌尿造口袋
Registration details
- Analysis ID
- fd89589b440e78d1413a172428df4f69
- Customs Code
- DHA04400202700
Company information
- Manufacturer
- COLOPLAST A/S
- Manufacturer Country
- Denmark
- Authorized Representative
- Taiwan Office of Hong Kong Commercial Coloplast Limited
Product details
- Intended Use
- It is used to collect stool or urine after an ileostomy, colostomy or urethrostomy.
- Product Type (Level 1)
- H Gastroenterology and urology
- Import Information
- import
Dates and status
- Registration Date
- Nov 07, 2005
- Expiry Date
- Nov 07, 2010
- Cancellation Date
- Nov 27, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Coloplast" Extra Large Urostomy Pocket in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fd89589b440e78d1413a172428df4f69 and manufactured by COLOPLAST A/S. The authorized representative in Taiwan is Taiwan Office of Hong Kong Commercial Coloplast Limited.
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.
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