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"Coloplast" Kangshuning Hernia Support Pair (Unsterilized) - Taiwan Registration 8a95d72402277f058420e9b5d842ba77

Access comprehensive regulatory information for "Coloplast" Kangshuning Hernia Support Pair (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8a95d72402277f058420e9b5d842ba77 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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8a95d72402277f058420e9b5d842ba77
Registration Details
Taiwan FDA Registration: 8a95d72402277f058420e9b5d842ba77
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Device Details

"Coloplast" Kangshuning Hernia Support Pair (Unsterilized)
TW: โ€œๅบทๆจ‚ไฟโ€ๅบทๆŸๅฏง็–่„ซๆ”ฏๆ’ๆŸ่คฒ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

8a95d72402277f058420e9b5d842ba77

DHA04400595909

Company Information

Product Details

Limited to the first level recognition range of the hernia brace (H.5970) of the Measures for the Administration of Medical Devices.

H Gastroenterology and urology

H.5970 Hernia Removal Supporter

import

Dates and Status

Jun 22, 2007

Jun 22, 2012

Apr 15, 2014

Cancellation Information

Logged out

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