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"Kenda" grinding series (unsterilized) - Taiwan Registration 91a4b5b5085189eae8bed23fb31c7687

Access comprehensive regulatory information for "Kenda" grinding series (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 91a4b5b5085189eae8bed23fb31c7687 and manufactured by KENDA AG VADUZ. The authorized representative in Taiwan is Sanye Limited.

This page provides complete technical specifications, regulatory compliance details. 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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91a4b5b5085189eae8bed23fb31c7687
Registration Details
Taiwan FDA Registration: 91a4b5b5085189eae8bed23fb31c7687
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Device Details

"Kenda" grinding series (unsterilized)
TW: "่‚ฏ้”" ็ ”็ฃจๆ็ณปๅˆ— (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

91a4b5b5085189eae8bed23fb31c7687

DHA04401034303

Company Information

Liechtenstein

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

import

Dates and Status

May 11, 2011

May 11, 2021

Jun 15, 2023

Cancellation Information

Logged out

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