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"Coloplast" post-operative pouch (unsterilized) - Taiwan Registration c0fc63407e745e442107f94e90e6191c

Access comprehensive regulatory information for "Coloplast" post-operative pouch (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c0fc63407e745e442107f94e90e6191c 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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c0fc63407e745e442107f94e90e6191c
Registration Details
Taiwan FDA Registration: c0fc63407e745e442107f94e90e6191c
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Device Details

"Coloplast" post-operative pouch (unsterilized)
TW: "ๅบทๆจ‚ไฟ" ๆ‰‹่ก“ๅพŒ็”จ้€ ๅฃ่ข‹ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

c0fc63407e745e442107f94e90e6191c

DHA04400155800

Company Information

Product Details

This product has a pouch attached to the patient's skin with adhesive material for the collection of stool or urine after an ileostomy, colostomy, or urethrostomy (an opening is surgically made in the surface of the small intestine, large intestine, or ureter).

H Gastroenterology and urology

H.5900 Stoma Bags and Accessories

import

Dates and Status

Oct 30, 2005

Oct 30, 2010

Nov 27, 2012

Cancellation Information

Logged out

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