Taiwan FDA registration 1333de171bdd986f204244f86b900603

"TRILUX" Medical Examination Light (Non-Sterile)

TW: "崔勒斯" 醫用檢查燈 (未滅菌)

Taiwan·Risk Class 1·MD·TRILUX MEDICAL GMBH & CO. KG·Registered Apr 24, 2017 – Apr 24, 2022Expired

Registration details

Analysis ID: 1333de171bdd986f204244f86b900603
License Form: Ministry of Health Medical Device Import No. 017750
Customs Code: DHA09401775005

Company information

Manufacturer: TRILUX MEDICAL GMBH & CO. KG
Manufacturer Country: Germany
Authorized Representative: T-SUN INTERNATIONAL CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Light Source for Optical Fiber Dentistry (F.4620)".
Product Type (Level 1): F Dental devices
Product Type (Level 2): F4620 Light source for photofiber dentistry
Import Information: Imported from abroad

Dates and status

Registration Date: Apr 24, 2017
Expiry Date: Apr 24, 2022

About this record

Access comprehensive regulatory information for "TRILUX" Medical Examination Light (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1333de171bdd986f204244f86b900603 and manufactured by TRILUX MEDICAL GMBH & CO. KG. The authorized representative in Taiwan is T-SUN INTERNATIONAL CO., LTD..

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