Taiwan FDA registration 65bab8f061c7362c89882d61957964a6

“INOHARA” Gutta Percha Points (Non-Sterile)

TW: “丼原”馬來膠針（未滅菌）

Taiwan·Risk Class 1·MD·Donbara International Co., Ltd. Pingzhen Factory·Registered Sep 19, 2018 – Sep 19, 2023Expired

Registration details

Analysis ID: 65bab8f061c7362c89882d61957964a6
License Form: Ministry of Health Medical Device Manufacturing No. 007439

Company information

Manufacturer: Donbara International Co., Ltd. Pingzhen Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: INOHARA DENTAL INSTRUMENT EQUIPMENT CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Malay Rubber (F.3850)".
Product Type (Level 1): F Dental devices
Product Type (Level 2): F3850 Male-Glue
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Sep 19, 2018
Expiry Date: Sep 19, 2023

About this record

Access comprehensive regulatory information for “INOHARA” Gutta Percha Points (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 65bab8f061c7362c89882d61957964a6 and manufactured by Donbara International Co., Ltd. Pingzhen Factory. The authorized representative in Taiwan is INOHARA DENTAL INSTRUMENT EQUIPMENT CO., LTD..

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