Taiwan FDA registration 9a7e19cd3eaa3a7621ecf9f0d99c2925

"Seton" multi-band lighting system

TW: “賽頓”多頻帶光照系統
Taiwan flagTaiwan·Risk Class 2·SCITON, INC.·Registered Sep 14, 2012 – Sep 14, 2017Cancelled
Registration details
Analysis ID
9a7e19cd3eaa3a7621ecf9f0d99c2925
Customs Code
DHA00602403001
Company information
Manufacturer
SCITON, INC.
Manufacturer Country
United States
Authorized Representative
DYNAMIC MEDICAL TECHNOLOGIES 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
import
Dates and status
Registration Date
Sep 14, 2012
Expiry Date
Sep 14, 2017
Cancellation Date
Dec 09, 2019
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 "Seton" multi-band lighting system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9a7e19cd3eaa3a7621ecf9f0d99c2925 and manufactured by SCITON, INC.. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SCITON, 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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