Taiwan FDA registration 4082e50abb319576cce35fb9313c8d7a

"Diou" CAD/CAM optical mold taking system (unsterilized)

TW: "帝歐" CAD/CAM光學取模系統 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·DIO CORPORATION·Registered Feb 04, 2016 – Feb 04, 2021Cancelled
Registration details
Analysis ID
4082e50abb319576cce35fb9313c8d7a
Customs Code
DHA09401614904
Company information
Manufacturer
DIO CORPORATION
Manufacturer Country
Korea, Republic of
Authorized Representative
DIO IMPLANT TAIWAN CORPORATION
Product details
Intended Use
Limited to the first level recognition range of CAD/CAM optical mold taking system (F.3661) for the management of medical equipment.
Product Type (Level 1)
F Dentistry
Product Type (Level 2)
F.3661 CAD/CAM光學取模系統
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Feb 04, 2016
Expiry Date
Feb 04, 2021
Cancellation Date
Sep 23, 2023
Cancellation information
Status
Logged out
Reason
自行鍵入
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About this record

Access comprehensive regulatory information for "Diou" CAD/CAM optical mold taking system (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4082e50abb319576cce35fb9313c8d7a and manufactured by DIO CORPORATION. The authorized representative in Taiwan is DIO IMPLANT TAIWAN CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DIO CORPORATION, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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