Taiwan FDA registration d4dc11abe192812aa989d3e4bba570e6

"MARY DIA" Dental diamond instrument (Non-Sterile)

TW: "日向和田" 牙科用鑽石器械 (未滅菌)

Taiwan·Risk Class 1·MD·HINATAWADA SEIMITSU MFG. CO., LTD.·Registered Jun 05, 2019 – Jun 05, 2024Expired

Registration details

Analysis ID: d4dc11abe192812aa989d3e4bba570e6
License Form: Ministry of Health Medical Device Import No. 020526
Customs Code: DHA09402052600

Company information

Manufacturer: HINATAWADA SEIMITSU MFG. CO., LTD.
Manufacturer Country: Japan
Authorized Representative: CHENSELECT CO., LTD.

Product details

Intended Use: Limited to the first level identification range of dental diamond instruments (F.4535) under the Measures for the Administration of Medical Equipment.
Product Type (Level 1): F Dental devices
Product Type (Level 2): F4535 Dental Diamond Instruments
Import Information: Imported from abroad

Dates and status

Registration Date: Jun 05, 2019
Expiry Date: Jun 05, 2024

About this record

Access comprehensive regulatory information for "MARY DIA" Dental diamond instrument (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 d4dc11abe192812aa989d3e4bba570e6 and manufactured by HINATAWADA SEIMITSU MFG. CO., LTD.. The authorized representative in Taiwan is CHENSELECT CO., LTD..

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