Taiwan FDA registration 1d4ed2db989cf7e583ff3795acc75da8
"CUTERA" Diagnostic condensing lens (Non-Sterile)
TW: "酷德拉"診斷用聚光鏡片(未滅菌)
Taiwan·Risk Class 1·MD·CUTERA, INC.·Registered Jul 20, 2017 – Jul 20, 2027ActiveRegistration details
- Analysis ID
- 1d4ed2db989cf7e583ff3795acc75da8
- License Form
- Ministry of Health Medical Device Import No. 018093
- Customs Code
- DHA09401809300
Company information
- Manufacturer
- CUTERA, INC.
- Manufacturer Country
- United States
- Authorized Representative
- AESOLUTION BIOMEDICAL CO. LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Diagnostic Condensing Lenses (M.1380)".
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1380 Diagnostic Condensing Lens
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 20, 2017
- Expiry Date
- Jul 20, 2027
About this record
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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