Taiwan FDA registration 5517bdbd9041208c5cad76a669d249ea
"MEDMONT" Keratoscope(Non-Sterile)
TW: "美膜" 角膜鏡(未滅菌)
Taiwan·Risk Class 1·MD·MEDMONT INTERNATIONAL PTY LTD·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- 5517bdbd9041208c5cad76a669d249ea
- License Form
- Ministry of Health Medical Device Import Registration No. 010462
- Customs Code
- DHA08401046208
Company information
- Manufacturer
- MEDMONT INTERNATIONAL PTY LTD
- Manufacturer Country
- Australia
- Authorized Representative
- BIOMEGA INSTRUMENT CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1350 Keatoscope
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for "MEDMONT" Keratoscope(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 5517bdbd9041208c5cad76a669d249ea and manufactured by MEDMONT INTERNATIONAL PTY LTD. The authorized representative in Taiwan is BIOMEGA INSTRUMENT CO., LTD..
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