Taiwan FDA registration b33dad573b5a2188e1962500a7d8e8a8
"Artinis" Transilluminator (Non-Sterile)
TW: "阿德尼斯" 血管透照器 (未滅菌)
Taiwan·Risk Class 1·MD·ARTINIS MEDICAL SYSTEMS·Registered Mar 22, 2017 – Mar 22, 2022ExpiredRegistration details
- Analysis ID
- b33dad573b5a2188e1962500a7d8e8a8
- License Form
- Ministry of Health Medical Device Import No. 017634
- Customs Code
- DHA09401763403
Company information
- Manufacturer
- ARTINIS MEDICAL SYSTEMS
- Manufacturer Country
- Netherlands
- Authorized Representative
- MICROSTAR INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Translucent Apparatus (M.1945)".
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1945 transillumination
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 22, 2017
- Expiry Date
- Mar 22, 2022
About this record
Access comprehensive regulatory information for "Artinis" Transilluminator (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 b33dad573b5a2188e1962500a7d8e8a8 and manufactured by ARTINIS MEDICAL SYSTEMS. The authorized representative in Taiwan is MICROSTAR INSTRUMENTS CO., LTD..
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