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"iJURA Vadent" dental hand instruments (unsterilized) - Taiwan Registration 1c72312e0922c6623e3b51fb8139784c

Access comprehensive regulatory information for "iJURA Vadent" dental hand instruments (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1c72312e0922c6623e3b51fb8139784c and manufactured by Ivoclar Vivadent Manufacturing GmbH;;IVOCLAR VIVADENT AG. The authorized representative in Taiwan is BioLaden Consultant Corp..

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including Ivoclar Vivadent, Inc.; IVOCLAR VIVADENT AG, IVOCLAR VIVADENT AG;; GEB. RENGGLI AG, and 5 recent registrations in the same category. 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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1c72312e0922c6623e3b51fb8139784c
Registration Details
Taiwan FDA Registration: 1c72312e0922c6623e3b51fb8139784c
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Device Details

"iJURA Vadent" dental hand instruments (unsterilized)
TW: โ€œ็พฉ็ฒๅ˜‰ๅ‰็“ฆ็™ป็‰นโ€็‰™็ง‘ๆ‰‹็”จๅ™จๆขฐ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

1c72312e0922c6623e3b51fb8139784c

DHA09402049206

Company Information

Product Details

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

F Dentistry

F.4565 ็‰™็ง‘ๆ‰‹็”จๅ™จๆขฐ

Input;; Contract manufacturing

Dates and Status

May 28, 2019

May 28, 2024

Aug 08, 2023

Cancellation Information

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