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"Dio" Dental hand instrument (Non-sterile) - Taiwan Registration 262130b28574d2a8d5854752041856ee

Access comprehensive regulatory information for "Dio" Dental hand instrument (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 262130b28574d2a8d5854752041856ee and manufactured by DIO CORPORATION. The authorized representative in Taiwan is DIO IMPLANT TAIWAN CORPORATION.

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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262130b28574d2a8d5854752041856ee
Registration Details
Taiwan FDA Registration: 262130b28574d2a8d5854752041856ee
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Device Details

"Dio" Dental hand instrument (Non-sterile)
TW: "ๅธๆญ" ็‰™็ง‘ๆ‰‹็”จๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

262130b28574d2a8d5854752041856ee

Ministry of Health Medical Device Import No. 020419

DHA09402041909

Company Information

Korea, Republic of

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Dental Hand Instruments (F.4565)".

F Dental devices

F4565 Hand instruments for dental use

Imported from abroad

Dates and Status

May 07, 2019

May 07, 2024