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"Distin" plaster removal device (unsterilized) - Taiwan Registration 6d972c40d0c9b90e3102751400977246

Access comprehensive regulatory information for "Distin" plaster removal device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6d972c40d0c9b90e3102751400977246 and manufactured by DE SOUTTER MEDICAL LTD. The authorized representative in Taiwan is CHAWEI 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.

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6d972c40d0c9b90e3102751400977246
Registration Details
Taiwan FDA Registration: 6d972c40d0c9b90e3102751400977246
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Device Details

"Distin" plaster removal device (unsterilized)
TW: "็‹„ๅธ็‰น" ็Ÿณ่†ๆ‹†้™คๅ™จๆขฐ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

6d972c40d0c9b90e3102751400977246

DHA09402316404

Company Information

United Kingdom

Product Details

Limited to the classification and grading management measures for medical equipment, gypsum removal equipment (N.5960) first grade identification range.

N Orthopedics

N.5960 ็Ÿณ่†ๆ‹†้™คๅ™จๆขฐ

Input;; QMS/QSD

Dates and Status

Jun 28, 2023

Jun 28, 2028