Taiwan FDA registration 3e1575f9e9a3cc066929b6de116eb7b6

"Qiancai" phototherapy instrument

TW: “千才”光療儀
Taiwan flagTaiwan·Risk Class 2·LIVERAGE TECHNOLOGY INC.·Registered May 31, 2011 – May 31, 2016Cancelled
Registration details
Analysis ID
3e1575f9e9a3cc066929b6de116eb7b6
Customs Code
DHY00500332104
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
LIVERAGE TECHNOLOGY INC.
Product details
Intended Use
VENUS I is blank below
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
Dates and status
Registration Date
May 31, 2011
Expiry Date
May 31, 2016
Cancellation Date
Aug 14, 2018
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
Companies making similar products

Top companies providing products similar to ""Qiancai" phototherapy instrument"

Recent registrations

Recently registered similar products

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 3e1575f9e9a3cc066929b6de116eb7b6 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.

Free DatabasePowered by Pure Global AI89,000+ Devices1 Competitors1 Recent Registrations