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"Shitek" carbon dioxide laser surgical instrument - Taiwan Registration 1fea000e199b09cacf5cb8eaec544754

Access comprehensive regulatory information for "Shitek" carbon dioxide laser surgical instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1fea000e199b09cacf5cb8eaec544754 and manufactured by STRATEK CO., LTD.. The authorized representative in Taiwan is Yixin International Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including STRATEK CO., LTD., and 1 recent registrations in the same category. 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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1fea000e199b09cacf5cb8eaec544754
Registration Details
Taiwan FDA Registration: 1fea000e199b09cacf5cb8eaec544754
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Device Details

"Shitek" carbon dioxide laser surgical instrument
TW: โ€œ็Ÿณ็‰นๅ…‹โ€ไบŒๆฐงๅŒ–็ขณ้›ทๅฐ„ๆ‰‹่ก“ๅ„€
Risk Class 2
Cancelled

Registration Details

1fea000e199b09cacf5cb8eaec544754

DHA00602060200

Company Information

Korea, Republic of

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

import

Dates and Status

Feb 25, 2010

Feb 25, 2015

Apr 13, 2018

Cancellation Information

Logged out

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