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"iJURA Vadent" dental hand instruments (unsterilized) - Taiwan Registration 3d042b2017b1ac3e89c22e969f3b5821

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 3d042b2017b1ac3e89c22e969f3b5821 and manufactured by Ivoclar Vivadent, Inc.; 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 AG;; GEB. RENGGLI AG, IVOCLAR VIVADENT AG;; Helmut Zepf Medizintechnik GmbH, 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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3d042b2017b1ac3e89c22e969f3b5821
Registration Details
Taiwan FDA Registration: 3d042b2017b1ac3e89c22e969f3b5821
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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

Registration Details

3d042b2017b1ac3e89c22e969f3b5821

DHA09402050604

Company Information

Philippines;;Liechtenstein

Product Details

Limited to the classification and grading management of medical equipment, the first level identification range of dental hand instruments (F.4565).

F Dentistry

F.4565 ็‰™็ง‘ๆ‰‹็”จๅ™จๆขฐ

Contract manufacturing;; input

Dates and Status

May 30, 2019

May 30, 2029