Taiwan FDA registration c22a2a6ea082837bed06494aaec60ebb

"Donohara" dental amalgam capsules (unsterilized)

TW: “丼原”牙科用汞齊膠囊(未滅菌)

Taiwan·Risk Class 1·INOHARA DENTAL INSTRUMENT EQUIPMENT CO., LTD.·Registered Mar 04, 2010 – Mar 04, 2020Cancelled

Registration details

Analysis ID: c22a2a6ea082837bed06494aaec60ebb

Company information

Manufacturer: INOHARA DENTAL INSTRUMENT EQUIPMENT CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: INOHARA DENTAL INSTRUMENT EQUIPMENT CO., LTD.

Product details

Intended Use: It is limited to the first level identification scope of dental amalgam capsules (F.3110) in the Administrative Measures for Medical Devices.
Product Type (Level 1): F Dentistry
Product Type (Level 2): F.3110 牙科用汞齊膠囊
Import Information: Domestic

Dates and status

Registration Date: Mar 04, 2010
Expiry Date: Mar 04, 2020
Cancellation Date: Aug 05, 2022

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Donohara" dental amalgam capsules (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c22a2a6ea082837bed06494aaec60ebb and manufactured by INOHARA DENTAL INSTRUMENT EQUIPMENT CO., LTD.. The authorized representative in Taiwan is INOHARA DENTAL INSTRUMENT EQUIPMENT CO., LTD..

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