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"DermLite" Speculum and accessories (Non-Sterile) - Taiwan Registration e9b6bfaf16fe787e8147c80c63249de2

Access comprehensive regulatory information for "DermLite" Speculum and accessories (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e9b6bfaf16fe787e8147c80c63249de2 and manufactured by DermLite, LLC. The authorized representative in Taiwan is GOLDENSPRING MEDI-TECH CO., LTD..

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e9b6bfaf16fe787e8147c80c63249de2
Registration Details
Taiwan FDA Registration: e9b6bfaf16fe787e8147c80c63249de2
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Device Details

"DermLite" Speculum and accessories (Non-Sterile)
TW: "ๅพท่Š็‰น" ๆชขๆŸฅ้กๅŠๅ…ถ้™„ไปถ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

e9b6bfaf16fe787e8147c80c63249de2

Ministry of Health Medical Device Import No. 022082

DHA09402208200

Company Information

United States

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Examination Scopes and Their Accessories (I.1800)".

I General and plastic surgical devices

I1800 inspection mirror and accessories

Imported from abroad

Dates and Status

Nov 04, 2020

Nov 04, 2025