"Aurora" Precision attachment (Non-Sterile) - Taiwan Registration debd8efc50fee81617c2cbcd5da703b3
Access comprehensive regulatory information for "Aurora" Precision attachment (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 debd8efc50fee81617c2cbcd5da703b3 and manufactured by AVINENT IMPLANT, SYSTEM, S.L.. The authorized representative in Taiwan is PORTLAND BIOTECHNICAL CO., LTD..
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Device Details
Registration Details
debd8efc50fee81617c2cbcd5da703b3
Ministry of Health Medical Device Import No. 022356
DHA09402235608
Product Details
Limited to the first level identification range of the "Precision Adhesive Body (F.3165)" of the Measures for the Administration of Medical Devices.
F Dental devices
F3165 precision bond
Imported from abroad
Dates and Status
Mar 04, 2021
Mar 04, 2026