Taiwan FDA registration 1fea000e199b09cacf5cb8eaec544754

"Shitek" carbon dioxide laser surgical instrument

TW: “石特克”二氧化碳雷射手術儀
Taiwan flagTaiwan·Risk Class 2·STRATEK CO., LTD.·Registered Feb 25, 2010 – Feb 25, 2015Cancelled
Registration details
Analysis ID
1fea000e199b09cacf5cb8eaec544754
Customs Code
DHA00602060200
Company information
Manufacturer
STRATEK CO., LTD.
Manufacturer Country
Korea, Republic of
Authorized Representative
Yixin International Co., Ltd
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4810 Lasers for general surgical, orthopaedic and dermatological use
Import Information
import
Dates and status
Registration Date
Feb 25, 2010
Expiry Date
Feb 25, 2015
Cancellation Date
Apr 13, 2018
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

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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