Taiwan FDA registration dbbd200f40fe94fd4f2dbf0de12d6042

"DENTSPLY Professional" Liquid medication dispenser (Non-Sterile)

TW: "登士派" 液體藥物給藥器 (未滅菌)

Taiwan·Risk Class 1·MD·DENTSPLY PROFESSIONAL·Registered May 23, 2014 – May 23, 2024Expired

Registration details

Analysis ID: dbbd200f40fe94fd4f2dbf0de12d6042
License Form: Ministry of Health Medical Device Import No. 014161
Customs Code: DHA09401416100

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 scope of the Measures for the Administration of Medical Devices "Liquid Drug Dispenser (J.6430)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J6430 Liquid drug applicator
Import Information: Imported from abroad

Dates and status

Registration Date: May 23, 2014
Expiry Date: May 23, 2024

About this record

Access comprehensive regulatory information for "DENTSPLY Professional" Liquid medication dispenser (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 dbbd200f40fe94fd4f2dbf0de12d6042 and manufactured by DENTSPLY PROFESSIONAL. The authorized representative in Taiwan is DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.).

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