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"Donohara" Malay gum needle (unsterilized) - Taiwan Registration 9c0f050624b0f3cb22fa257d5caa60f7

Access comprehensive regulatory information for "Donohara" Malay gum needle (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9c0f050624b0f3cb22fa257d5caa60f7 and manufactured by INOHARA DENTAL INSTRUMENT EQUIPMENT CO., LTD.. 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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9c0f050624b0f3cb22fa257d5caa60f7
Registration Details
Taiwan FDA Registration: 9c0f050624b0f3cb22fa257d5caa60f7
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Device Details

"Donohara" Malay gum needle (unsterilized)
TW: โ€œไธผๅŽŸโ€้ฆฌไพ†่† ้‡๏ผˆๆœชๆป…่Œ๏ผ‰
Risk Class 1
Cancelled

Registration Details

9c0f050624b0f3cb22fa257d5caa60f7

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 Dentistry

F.3850 Malay gum

Domestic

Dates and Status

Dec 05, 2013

Dec 05, 2018

Aug 05, 2022

Cancellation Information

Logged out

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