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“Ivoclar Vivadent”Resin Impression Tray Material (Non-Sterile) - Taiwan Registration e6d65cf9071976e1e7ca601dd81d9bf5

Access comprehensive regulatory information for “Ivoclar Vivadent”Resin Impression Tray Material (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e6d65cf9071976e1e7ca601dd81d9bf5 and manufactured by IVOCLAR VIVADENT, INC.. The authorized representative in Taiwan is BioLaden Consultant Corp..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including IVOCLAR VIVADENT AG, and 1 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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e6d65cf9071976e1e7ca601dd81d9bf5
Registration Details
Taiwan FDA Registration: e6d65cf9071976e1e7ca601dd81d9bf5
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Device Details

“Ivoclar Vivadent”Resin Impression Tray Material (Non-Sterile)
TW: “義獲嘉偉瓦登特”樹脂印模牙托材(未滅菌)
Risk Class 1
MD

Registration Details

e6d65cf9071976e1e7ca601dd81d9bf5

Ministry of Health Medical Device Import Registration No. 009449

DHA08400944903

Company Information

United States

Product Details

Limited to the first level identification range of resin impression dental tray (F.3670) of the management method for medical equipment.

F Dental devices

F3670 resin impression dental tray

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026

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