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"INOHARA" Endodontic Paper Points (Non-Sterile) - Taiwan Registration 8559989ef03ead6f21295b41255e53fb

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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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8559989ef03ead6f21295b41255e53fb
Registration Details
Taiwan FDA Registration: 8559989ef03ead6f21295b41255e53fb
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Device Details

"INOHARA" Endodontic Paper Points (Non-Sterile)
TW: "ไธผๅŽŸ" ๆ น็ฎก็ด™้‡ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

8559989ef03ead6f21295b41255e53fb

Ministry of Health Medical Device Manufacturing No. 006698

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Root Canal Paper Needle (F.3830)".

F Dental devices

F3830 tube paper needle

Produced in Taiwan, China

Dates and Status

Apr 21, 2017

Apr 21, 2022