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"Renver" multi-dense printing mold automatic mixer (unsterilized) - Taiwan Registration 6c79e21d51bd9c783f9714b5bb479e21

Access comprehensive regulatory information for "Renver" multi-dense printing mold automatic mixer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6c79e21d51bd9c783f9714b5bb479e21 and manufactured by RENFERT GMBH. The authorized representative in Taiwan is DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.).

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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6c79e21d51bd9c783f9714b5bb479e21
Registration Details
Taiwan FDA Registration: 6c79e21d51bd9c783f9714b5bb479e21
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Device Details

"Renver" multi-dense printing mold automatic mixer (unsterilized)
TW: โ€œๅ€ซไฝ›โ€ๅคš่€Œๅฏ†ๅฐๆจกๆ่‡ชๅ‹•ๆททๅˆๆฉŸ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

6c79e21d51bd9c783f9714b5bb479e21

DHA04400582300

Company Information

Germany

Product Details

Limited to the first level identification range of dental and mercury instruments (F.3100) in the management of medical devices.

F Dentistry

F.3100 Dental and mercury appliances

import

Dates and Status

May 04, 2007

May 04, 2022

Apr 12, 2024

Cancellation Information

Logged out

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