"iJURA Vadent" resin applicator (unsterilized) - Taiwan Registration 5841e3858d3e628a0b3c3850ac3c10ed
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 5841e3858d3e628a0b3c3850ac3c10ed and manufactured by IVOCLAR VIVADENT INC. (IVPH);;IVOCLAR VIVADENT AG. The authorized representative in Taiwan is BioLaden Consultant Corp..
This page provides complete technical specifications, regulatory compliance details, 3 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.
Device Details
Registration Details
5841e3858d3e628a0b3c3850ac3c10ed
DHA08401910707
Product Details
Limited to the first level identification range of resin applicator (F.3140) of the classification and grading management method of medical equipment.
F Dentistry
F.3140 Resin Coating Machine
Input;; Contract manufacturing
Dates and Status
Oct 01, 2021
Oct 31, 2023
Nov 02, 2023
Cancellation Information
Logged out
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"iJURA Vadent" resin applicator (unsterilized)
Gebr. Renggli AG;;IVOCLAR VIVADENT AG
7637950881cfc1b0b74ea8464a728d4e
1
"iJURA Vadent" resin applicator (unsterilized)
IVOCLAR VIVADENT INC. (IVPH);;IVOCLAR VIVADENT AG
8cd61c4bb0411863662950d5239cbf1d
1
"iJURA Vadent" resin applicator (unsterilized)
IVOCLAR VIVADENT AG
53636e67b0cd4aece61b424777708e86
1

