Taiwan FDA registration 2b823cbfe0bc733cf4c9fc86e140d897

"Diou" scan locator (unsterilized)

TW: "帝歐" 掃描定位體 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·DIO CORPORATION·Registered Oct 01, 2021 – Oct 31, 2027Active
Registration details
Analysis ID
2b823cbfe0bc733cf4c9fc86e140d897
Customs Code
DHA08401732507
Company information
Manufacturer
DIO CORPORATION
Manufacturer Country
Korea, Republic of
Authorized Representative
DIO IMPLANT TAIWAN CORPORATION
Product details
Intended Use
Limited to the classification and grading management method of medical equipment, CAD/CAM optical mold taking system (F.3661) first level recognition range.
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
Oct 01, 2021
Expiry Date
Oct 31, 2027
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About this record

Access comprehensive regulatory information for "Diou" scan locator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2b823cbfe0bc733cf4c9fc86e140d897 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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