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"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.

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5841e3858d3e628a0b3c3850ac3c10ed
Registration Details
Taiwan FDA Registration: 5841e3858d3e628a0b3c3850ac3c10ed
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Device Details

"iJURA Vadent" resin applicator (unsterilized)
TW: "็พฉ็ฒๅ˜‰ๅ‰็“ฆ็™ป็‰น" ๆจน่„‚ๅก—ๆ•ทๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

5841e3858d3e628a0b3c3850ac3c10ed

DHA08401910707

Company Information

Philippines;;Liechtenstein

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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