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"Vericom" EDTA Root Canal Preparator (Non-Sterile) - Taiwan Registration 005d86be3434f3042b4e051a058d444b

Access comprehensive regulatory information for "Vericom" EDTA Root Canal Preparator (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 005d86be3434f3042b4e051a058d444b and manufactured by VERICOM CO., LTD.. The authorized representative in Taiwan is SUNDENT CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including VERICOM CO., LTD., 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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005d86be3434f3042b4e051a058d444b
Registration Details
Taiwan FDA Registration: 005d86be3434f3042b4e051a058d444b
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Device Details

"Vericom" EDTA Root Canal Preparator (Non-Sterile)
TW: "่‘ณ็ˆพๅบท" ๆ น็ฎกๆ“ดๅคงๆ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

005d86be3434f3042b4e051a058d444b

Ministry of Health Medical Device Import No. 017788

DHA09401778804

Company Information

Korea, Republic of

Product Details

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

F Dental devices

F4565 Hand instruments for dental use

Imported from abroad

Dates and Status

May 04, 2017

May 04, 2027

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