Taiwan FDA registration 6da921d515181649631f0c2eabd44bc4

"Jiexi" phototherapy instrument

TW: “婕曦”光療儀
Taiwan flagTaiwan·Risk Class 2·Jeisys Medical Inc.·Registered Mar 03, 2010 – Mar 03, 2020Cancelled
Registration details
Analysis ID
6da921d515181649631f0c2eabd44bc4
Customs Code
DHA00602062502
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
Mar 03, 2010
Expiry Date
Mar 03, 2020
Cancellation Date
Oct 05, 2020
Cancellation information
Status
Logged out
Reason
自請註銷;;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 6da921d515181649631f0c2eabd44bc4 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, 2 companies making similar products including Jeisys Medical Inc., 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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