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"Illipus" shuttle laser hand grip - Taiwan Registration 96233c119a50366c403855da78525395

Access comprehensive regulatory information for "Illipus" shuttle laser hand grip in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 96233c119a50366c403855da78525395 and manufactured by ELLIPSE A/S. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..

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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96233c119a50366c403855da78525395
Registration Details
Taiwan FDA Registration: 96233c119a50366c403855da78525395
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Device Details

"Illipus" shuttle laser hand grip
TW: โ€œไผŠๅˆฉๆ™ฎๆ–ฏโ€้ฃ›ๆขญ้›ทๅฐ„ๆ‰‹ๆกๆŠŠ
Risk Class 2
Cancelled

Registration Details

96233c119a50366c403855da78525395

DHA05602946301

Company Information

Denmark

Product Details

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

I General, Plastic Surgery and Dermatology

I.4810 Lasers for general surgical, orthopaedic and dermatological use

Input;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.

Dates and Status

Feb 22, 2017

Feb 22, 2022

Apr 12, 2024

Cancellation Information

Logged out

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