Taiwan FDA registration 7637950881cfc1b0b74ea8464a728d4e

"iJURA Vadent" resin applicator (unsterilized)

TW: "義獲嘉偉瓦登特" 樹脂塗敷器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Gebr. Renggli AG;;IVOCLAR VIVADENT AG·Registered Jul 05, 2023 – Oct 31, 2025Expired
Registration details
Analysis ID
7637950881cfc1b0b74ea8464a728d4e
Customs Code
DHA084a0019907
Company information
Manufacturer Country
Liechtenstein;;Switzerland
Authorized Representative
BioLaden Consultant Corp.
Product details
Intended Use
Limited to the first level identification range of resin applicator (F.3140) of the classification and grading management method of medical equipment.
Product Type (Level 1)
F Dentistry
Product Type (Level 2)
F.3140 Resin Coating Machine
Dates and status
Registration Date
Jul 05, 2023
Expiry Date
Oct 31, 2025
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About this record

Access comprehensive regulatory information for "iJURA Vadent" resin applicator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7637950881cfc1b0b74ea8464a728d4e and manufactured by Gebr. Renggli AG;;IVOCLAR VIVADENT AG. The authorized representative in Taiwan is BioLaden Consultant Corp..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including IVOCLAR VIVADENT INC. (IVPH);;IVOCLAR VIVADENT AG, IVOCLAR VIVADENT AG, and 3 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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