Taiwan FDA registration 8559989ef03ead6f21295b41255e53fb

"INOHARA" Endodontic Paper Points (Non-Sterile)

TW: "丼原" 根管紙針 (未滅菌)

Taiwan·Risk Class 1·MD·Donbara International Co., Ltd. Pingzhen Factory·Registered Apr 21, 2017 – Apr 21, 2022Expired

Registration details

Analysis ID: 8559989ef03ead6f21295b41255e53fb
License Form: Ministry of Health Medical Device Manufacturing No. 006698

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 range of the Measures for the Administration of Medical Devices "Root Canal Paper Needle (F.3830)".
Product Type (Level 1): F Dental devices
Product Type (Level 2): F3830 tube paper needle
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Apr 21, 2017
Expiry Date: Apr 21, 2022

About this record

Access comprehensive regulatory information for "INOHARA" Endodontic Paper 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 8559989ef03ead6f21295b41255e53fb 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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