Taiwan FDA registration 09e6e3cb3a46bcee6ebe87364d52c806

"Dretta" root canal center column nail (unsterilized)

TW: "德瑞塔" 根管中心柱釘 (未滅菌)

Taiwan·Risk Class 1·DIRECT AB·Registered Dec 20, 2010 – Dec 20, 2025Expired

Registration details

Analysis ID: 09e6e3cb3a46bcee6ebe87364d52c806
Customs Code: DHA04400971300

Company information

Manufacturer: DIRECT AB
Manufacturer Country: Sweden
Authorized Representative: SHIN YEAN TRADING CO., LTD.

Product details

Intended Use: It is limited to the first-level identification scope of the "Root Canal Center Pillar (F.3810)" of the Classification and Grading Management Measures for Medical Devices.
Product Type (Level 1): F Dentistry
Product Type (Level 2): F.3810 Root canal center post
Import Information: import

Dates and status

Registration Date: Dec 20, 2010
Expiry Date: Dec 20, 2025

About this record

Access comprehensive regulatory information for "Dretta" root canal center column nail (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 09e6e3cb3a46bcee6ebe87364d52c806 and manufactured by DIRECT AB. The authorized representative in Taiwan is SHIN YEAN TRADING CO., LTD..

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