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"J. Morita" Dentaport Root ZX Module (non-Sterile) - Taiwan Registration 0a04422e6111c72856979a85d41787dd

Access comprehensive regulatory information for "J. Morita" Dentaport Root ZX Module (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 0a04422e6111c72856979a85d41787dd and manufactured by J. MORITA MFG. CORP.. The authorized representative in Taiwan is FOMED BIOTECH 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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0a04422e6111c72856979a85d41787dd
Registration Details
Taiwan FDA Registration: 0a04422e6111c72856979a85d41787dd
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Device Details

"J. Morita" Dentaport Root ZX Module (non-Sterile)
TW: "ๆ—ฅๆœฌๆฃฎ็”ฐ" ๆ น็ฎก้•ทๅบฆๆธฌ้‡ๅ„€(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

0a04422e6111c72856979a85d41787dd

Ministry of Health Medical Device Import No. 019090

DHA09401909002

Company Information

Japan

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 Dental devices

F6640 Dental Surgical Devices and Their Accessories

Imported from abroad

Dates and Status

May 24, 2018

May 24, 2028