Taiwan FDA registration fd296733f8ce7f862bddb26d29b6addd

"Jiexi" phototherapy instrument

TW: “婕曦”光療儀
Taiwan flagTaiwan·Risk Class 2·JEISYS MEDICAL INC.·Registered Nov 05, 2009 – Nov 05, 2014Cancelled
Registration details
Analysis ID
fd296733f8ce7f862bddb26d29b6addd
Customs Code
DHA00602029504
Company information
Manufacturer Country
Korea, Republic of
Authorized Representative
VICTORY EIGHT ENTERPRISE 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
Nov 05, 2009
Expiry Date
Nov 05, 2014
Cancellation Date
May 28, 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 "Jiexi" 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 fd296733f8ce7f862bddb26d29b6addd and manufactured by JEISYS MEDICAL INC.. The authorized representative in Taiwan is VICTORY EIGHT ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Jeisys Medical Inc., and 3 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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