Taiwan FDA registration d21d7067ca5439531063c5374a641806

"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·Bridge2, LLC (Young Microbrush LLC);;IVOCLAR VIVADENT AG·Registered Mar 20, 2019 – Mar 20, 2029Active
Registration details
Analysis ID
d21d7067ca5439531063c5374a641806
Customs Code
DHA09402021608
Company information
Manufacturer Country
Liechtenstein;;United States
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
Mar 20, 2019
Expiry Date
Mar 20, 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 d21d7067ca5439531063c5374a641806 and manufactured by Bridge2, LLC (Young Microbrush LLC);;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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