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"Erdenta" grinding device and its accessories (unsterilized) - Taiwan Registration bf84265da38aba70859b92cd1eda0830

Access comprehensive regulatory information for "Erdenta" 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 bf84265da38aba70859b92cd1eda0830 and manufactured by EDENTA AG. The authorized representative in Taiwan is MIDST ENTERPRISE CO., LTD.

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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bf84265da38aba70859b92cd1eda0830
Registration Details
Taiwan FDA Registration: bf84265da38aba70859b92cd1eda0830
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Device Details

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

Registration Details

bf84265da38aba70859b92cd1eda0830

DHA04401227802

Company Information

Switzerland

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

Oct 19, 2012

Oct 19, 2017

Dec 20, 2019

Cancellation Information

Logged out

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