Taiwan FDA registration a45a142c23809b608e72862abfed5c61

Icura Vita Wadent grinding unit and its accessories (unsterilized)

TW: “義獲嘉偉瓦登特”研磨裝置及其附件(未滅菌)
Taiwan flagTaiwan·Risk Class 1·EVE Ernst Vetter GmbH;;IVOCLAR VIVADENT AG·Registered Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
a45a142c23809b608e72862abfed5c61
Customs Code
DHA08402028100
Company information
Manufacturer Country
Liechtenstein;;Germany
Authorized Representative
BioLaden Consultant Corp.
Product details
Intended Use
Limited to the first level identification range of grinding devices and their accessories (F.6010) of the classification and grading management methods for medical equipment.
Product Type (Level 1)
F Dentistry
Product Type (Level 2)
F.6010 Abrasive devices and accessories thereof
Import Information
Input;; Contract manufacturing
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2025
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About this record

Access comprehensive regulatory information for Icura Vita Wadent grinding unit and its accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a45a142c23809b608e72862abfed5c61 and manufactured by EVE Ernst Vetter GmbH;;IVOCLAR VIVADENT AG. The authorized representative in Taiwan is BioLaden Consultant Corp..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including EVE Ernst Vetter GmbH;;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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