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"Disi" dental surgical device and its accessories (unsterilized) - Taiwan Registration 87cbc4c72a1bd3ac1039c6b3ca709664

Access comprehensive regulatory information for "Disi" dental surgical 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 87cbc4c72a1bd3ac1039c6b3ca709664 and manufactured by DCI EQUIPMENT. The authorized representative in Taiwan is Taiwan Kava 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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87cbc4c72a1bd3ac1039c6b3ca709664
Registration Details
Taiwan FDA Registration: 87cbc4c72a1bd3ac1039c6b3ca709664
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Device Details

"Disi" dental surgical device and its accessories (unsterilized)
TW: "่ฟชๆ€่‰พ"็‰™็ง‘ๆ‰‹่ก“่ฃ็ฝฎๅŠๅ…ถ้™„ไปถ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

87cbc4c72a1bd3ac1039c6b3ca709664

DHA04401288306

Company Information

United States

Product Details

Limited to the first level identification range of dental surgical devices and their accessories (F.6640) under the Measures for the Administration of Medical Devices.

F Dentistry

F.6640 Dental surgical devices and accessories thereof

import

Dates and Status

Apr 10, 2013

Apr 10, 2018

Mar 01, 2018

Cancellation Information

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