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"Chimead" Terrilang attached to a syringe - Taiwan Registration 2e0604d724f21989186390a5c72b5435

Access comprehensive regulatory information for "Chimead" Terrilang attached to a syringe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 2e0604d724f21989186390a5c72b5435 and manufactured by Q-MED AB. The authorized representative in Taiwan is GALDERMA HONG KONG LIMITED, TAIWAN BRANCH.

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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2e0604d724f21989186390a5c72b5435
Registration Details
Taiwan FDA Registration: 2e0604d724f21989186390a5c72b5435
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Device Details

"Chimead" Terrilang attached to a syringe
TW: โ€œๅฅ‡็พŽๅพทโ€็‰น้บ—ๆœ—้™„ๆณจๅฐ„ๅ™จ
Risk Class 3
Cancelled

Registration Details

2e0604d724f21989186390a5c72b5435

DHA00602297500

Company Information

Sweden

Product Details

For details, it is Chinese approved copy of the imitation order

I General, Plastic Surgery and Dermatology

import

Dates and Status

Oct 27, 2011

Oct 27, 2016

May 14, 2018

Cancellation Information

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