Taiwan FDA registration 30129c15b2e8c2021d8d55beed17776b

"Qiancai" phototherapy instrument

TW: “千才”光療儀
Taiwan flagTaiwan·Risk Class 2·LIVERAGE TECHNOLOGY INC.·Registered Jan 09, 2017 – Jan 09, 2027Active
Registration details
Analysis ID
30129c15b2e8c2021d8d55beed17776b
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
LIVERAGE TECHNOLOGY INC.
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
Domestic;; 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
Registration Date
Jan 09, 2017
Expiry Date
Jan 09, 2027
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About this record

Access comprehensive regulatory information for "Qiancai" phototherapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 30129c15b2e8c2021d8d55beed17776b and manufactured by LIVERAGE TECHNOLOGY INC.. The authorized representative in Taiwan is LIVERAGE TECHNOLOGY INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LIVERAGE TECHNOLOGY INC., 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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