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"De Tower" dental equipment (unsterilized) - Taiwan Registration 416ee5507d73f47994f0ae1dab5a4bf7

Access comprehensive regulatory information for "De Tower" dental equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 416ee5507d73f47994f0ae1dab5a4bf7 and manufactured by DIRECT AB. The authorized representative in Taiwan is ADVANCE DEVELOPMENT INC..

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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416ee5507d73f47994f0ae1dab5a4bf7
Registration Details
Taiwan FDA Registration: 416ee5507d73f47994f0ae1dab5a4bf7
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Device Details

"De Tower" dental equipment (unsterilized)
TW: โ€œๅพ—ๆ“‚ๅก”โ€็‰™็ง‘็”จๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

416ee5507d73f47994f0ae1dab5a4bf7

DHA04400692803

Company Information

Sweden

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Dental Hand Instruments (F.4565)".

F Dentistry

F.4565 ็‰™็ง‘ๆ‰‹็”จๅ™จๆขฐ

import

Dates and Status

Jul 16, 2008

Jul 16, 2018

Jun 17, 2022

Cancellation Information

Logged out

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