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"DENTSPLY Professional" Liquid medication dispenser (Non-Sterile) - Taiwan Registration dbbd200f40fe94fd4f2dbf0de12d6042

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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dbbd200f40fe94fd4f2dbf0de12d6042
Registration Details
Taiwan FDA Registration: dbbd200f40fe94fd4f2dbf0de12d6042
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Device Details

"DENTSPLY Professional" Liquid medication dispenser (Non-Sterile)
TW: "็™ปๅฃซๆดพ" ๆถฒ้ซ”่—ฅ็‰ฉ็ตฆ่—ฅๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

dbbd200f40fe94fd4f2dbf0de12d6042

Ministry of Health Medical Device Import No. 014161

DHA09401416100

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Liquid Drug Dispenser (J.6430)".

J General hospital and personal use equipment

J6430 Liquid drug applicator

Imported from abroad

Dates and Status

May 23, 2014

May 23, 2024