Taiwan FDA registration 2d0531c0cddddc3e3110b2b31d8f4401
"Straight Cap" Dental Procedure Guide Plate (Unsterilized)
TW: “植直蓋”牙科手術導引板 (未滅菌)
Taiwan·Risk Class 1·SHINEO TECHNOLOGY CO., LTD.·Registered Dec 21, 2017 – Dec 21, 2027ActiveRegistration details
- Analysis ID
- 2d0531c0cddddc3e3110b2b31d8f4401
Company information
- Manufacturer
- SHINEO TECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ENLIGHTEN MATERIALS CO., LTD
Product details
- Intended Use
- Limited to the classification and grading management measures of medical equipment "Dental Bone Implant Operation Equipment (F.3980)" Identification Scope of the First Level.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3980 Intradental implant manipulation equipment
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Dec 21, 2017
- Expiry Date
- Dec 21, 2027
About this record
Access comprehensive regulatory information for "Straight Cap" Dental Procedure Guide Plate (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2d0531c0cddddc3e3110b2b31d8f4401 and manufactured by SHINEO TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is ENLIGHTEN MATERIALS CO., LTD.
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