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"Tister" plaster removal device (unsterilized) - Taiwan Registration 944103344d5b726574415dced6a0e1ff

Access comprehensive regulatory information for "Tister" 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 944103344d5b726574415dced6a0e1ff and manufactured by DE SOUTTER MEDICAL LIMITED. The authorized representative in Taiwan is PRO-READY ENTERPRISE 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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944103344d5b726574415dced6a0e1ff
Registration Details
Taiwan FDA Registration: 944103344d5b726574415dced6a0e1ff
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Device Details

"Tister" plaster removal device (unsterilized)
TW: โ€œ่’‚ๆฐ็‰นโ€็Ÿณ่†ๆ‹†้™คๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

944103344d5b726574415dced6a0e1ff

DHA04401183901

Company Information

United Kingdom

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Gypsum Removal Devices (N.5960)".

N Orthopedics

N.5960 ็Ÿณ่†ๆ‹†้™คๅ™จๆขฐ

import

Dates and Status

Jun 18, 2012

Jun 18, 2022

Apr 12, 2024

Cancellation Information

Logged out

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