Taiwan FDA registration dd5876a2d3fbe377507a0565b48addf0

"Professional" Fiber optic dental light (Non-sterile)

TW: "普菲納" 光纖維牙科用光源 (未滅菌)

Taiwan·Risk Class 1·MD·DENTSPLY PROFESSIONAL·Registered Sep 20, 2017 – Sep 20, 2022Expired

Registration details

Analysis ID: dd5876a2d3fbe377507a0565b48addf0
License Form: Ministry of Health Medical Device Import No. 018334
Customs Code: DHA09401833409

Company information

Manufacturer: DENTSPLY PROFESSIONAL
Manufacturer Country: United States
Authorized Representative: DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.)

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: Sep 20, 2017
Expiry Date: Sep 20, 2022

About this record

Access comprehensive regulatory information for "Professional" Fiber optic dental 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 dd5876a2d3fbe377507a0565b48addf0 and manufactured by DENTSPLY PROFESSIONAL. The authorized representative in Taiwan is DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.).

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