"CUTERA" Diagnostic condensing lens (Non-Sterile) - Taiwan Registration 1d4ed2db989cf7e583ff3795acc75da8
Access comprehensive regulatory information for "CUTERA" Diagnostic condensing lens (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 1d4ed2db989cf7e583ff3795acc75da8 and manufactured by CUTERA, INC.. The authorized representative in Taiwan is AESOLUTION BIOMEDICAL CO. LTD..
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Device Details
Registration Details
1d4ed2db989cf7e583ff3795acc75da8
Ministry of Health Medical Device Import No. 018093
DHA09401809300
Product Details
Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Diagnostic Condensing Lenses (M.1380)".
M Ophthalmic devices
M1380 Diagnostic Condensing Lens
Imported from abroad
Dates and Status
Jul 20, 2017
Jul 20, 2027