Taiwan FDA registration f5da09e7922983edff6aff9a2d8fb9c9

"iJURA Vadent" dental hand instruments (unsterilized)

TW: “義獲嘉偉瓦登特”牙科手用器械(未滅菌)
Taiwan flagTaiwan·Risk Class 1·SFS intec AG, Kunststoffwerk;;IVOCLAR VIVADENT AG·Registered Jun 06, 2019 – Jun 06, 2029Active
Registration details
Analysis ID
f5da09e7922983edff6aff9a2d8fb9c9
Customs Code
DHA09402052903
Company information
Manufacturer Country
Liechtenstein;;Switzerland
Authorized Representative
BioLaden Consultant Corp.
Product details
Intended Use
Limited to the classification and grading management of medical equipment, the first level identification range of dental hand instruments (F.4565).
Product Type (Level 1)
F Dentistry
Product Type (Level 2)
F.4565 牙科手用器械
Import Information
Contract manufacturing;; input
Dates and status
Registration Date
Jun 06, 2019
Expiry Date
Jun 06, 2029
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About this record

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 f5da09e7922983edff6aff9a2d8fb9c9 and manufactured by SFS intec AG, Kunststoffwerk;;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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