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"Weida" grinding device and its accessories (unsterilized) - Taiwan Registration 08cb9fdb20a302e82aca92bd01299e80

Access comprehensive regulatory information for "Weida" grinding device 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 08cb9fdb20a302e82aca92bd01299e80 and manufactured by EVE Ernst Vetter GmbH;; VITA Zahnfabrik H. Rauter GmbH & CO. KG. The authorized representative in Taiwan is TESCO DENTAL ASIA LIMITED TAIWAN BRANCH (H.K.).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including EVE Ernst Vetter GmbH;; VITA Zahnfabrik H. Rauter GmbH & CO. KG, 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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08cb9fdb20a302e82aca92bd01299e80
Registration Details
Taiwan FDA Registration: 08cb9fdb20a302e82aca92bd01299e80
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Device Details

"Weida" grinding device and its accessories (unsterilized)
TW: โ€œๅ‰้”โ€็ ”็ฃจ่ฃ็ฝฎๅŠๅ…ถ้™„ไปถ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

08cb9fdb20a302e82aca92bd01299e80

DHA09401964202

Product Details

Limited to the first level identification range of grinding devices and their accessories (F.6010) under the management measures for medical equipment.

F Dentistry

F.6010 Abrasive devices and accessories thereof

Input;; Contract manufacturing

Dates and Status

Sep 26, 2018

Sep 26, 2023

Sep 30, 2021

Cancellation Information

Logged out

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