Taiwan FDA registration f0954249ac5bfde8c4899bf6712f9789

"Yoshioka" Precision Attachment (Non-Sterile)

TW: "吉岡" 精密接著體 (未滅菌)

Taiwan·Risk Class 1·MD·NEOMAX ENGINEERING CO., LTD.·Registered Jun 14, 2017 – Jun 14, 2022Expired

Registration details

Analysis ID: f0954249ac5bfde8c4899bf6712f9789
License Form: Ministry of Health Medical Device Import No. 017955
Customs Code: DHA09401795500

Company information

Manufacturer: NEOMAX ENGINEERING CO., LTD.
Manufacturer Country: Japan
Authorized Representative: YOSHIOKA CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the "Precision Adhesive Body (F.3165)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1): F Dental devices
Product Type (Level 2): F3165 precision bond
Import Information: Imported from abroad

Dates and status

Registration Date: Jun 14, 2017
Expiry Date: Jun 14, 2022

About this record

Access comprehensive regulatory information for "Yoshioka" Precision Attachment (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 f0954249ac5bfde8c4899bf6712f9789 and manufactured by NEOMAX ENGINEERING CO., LTD.. The authorized representative in Taiwan is YOSHIOKA CO., LTD..

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