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"Vericom" Surgical Guide (Non-Sterile) - Taiwan Registration 50f494d726ab522166548d4c1552d98f

Access comprehensive regulatory information for "Vericom" Surgical Guide (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 50f494d726ab522166548d4c1552d98f and manufactured by VERICOM CO., LTD.. The authorized representative in Taiwan is SUNDENT CORPORATION.

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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50f494d726ab522166548d4c1552d98f
Registration Details
Taiwan FDA Registration: 50f494d726ab522166548d4c1552d98f
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Device Details

"Vericom" Surgical Guide (Non-Sterile)
TW: "่‘ณ็ˆพๅบท" ๆ‰‹่ก“ๅฐŽๆฟ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

50f494d726ab522166548d4c1552d98f

Ministry of Health Medical Device Import No. 021999

DHA09402199906

Company Information

Korea, Republic of

Product Details

Limited to the first-level identification scope of the Measures for the Administration of Medical Devices "Dental Implant Attachment (F.3980)".

F Dental devices

F3980 Dental Intraosseous Implant Attachment

Imported from abroad

Dates and Status

Sep 28, 2020

Sep 28, 2025