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“INOHARA” Gutta Percha Points (Non-Sterile) - Taiwan Registration 65bab8f061c7362c89882d61957964a6

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..

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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65bab8f061c7362c89882d61957964a6
Registration Details
Taiwan FDA Registration: 65bab8f061c7362c89882d61957964a6
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Device Details

“INOHARA” Gutta Percha Points (Non-Sterile)
TW: “丼原”馬來膠針(未滅菌)
Risk Class 1
MD

Registration Details

65bab8f061c7362c89882d61957964a6

Ministry of Health Medical Device Manufacturing No. 007439

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Malay Rubber (F.3850)".

F Dental devices

F3850 Male-Glue

Produced in Taiwan, China

Dates and Status

Sep 19, 2018

Sep 19, 2023