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"Coloplast" stoma chassis after surgery (unsterilized) - Taiwan Registration 530d7077d4cb55fe11592e890a2725c7

Access comprehensive regulatory information for "Coloplast" stoma chassis after surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 530d7077d4cb55fe11592e890a2725c7 and manufactured by COLOPLAST HUNGARY LTD. 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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530d7077d4cb55fe11592e890a2725c7
Registration Details
Taiwan FDA Registration: 530d7077d4cb55fe11592e890a2725c7
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Device Details

"Coloplast" stoma chassis after surgery (unsterilized)
TW: "ๅบทๆจ‚ไฟ" ๆ‰‹่ก“ๅพŒ็”จ้€ ๅฃๅบ•็›ค(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

530d7077d4cb55fe11592e890a2725c7

DHA04400172707

Company Information

Product Details

The ostomy bag and its attachments contain a bag attached to the skin with adhesive material to collect stool or urine after an ileostomy, colostomy, or urethrostomy (a surgical opening in the small intestine, large intestine, or ureter).

H Gastroenterology and urology

import

Dates and Status

Nov 03, 2005

Nov 03, 2010

Nov 27, 2012

Cancellation Information

Logged out

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