Taiwan FDA registration bd5406cd99c4f614aae522e60001c7bf
"M.I.ONE" EAR, NOSE, AND THROAT FIBEROPTIC LIGHT SOURCE AND CARRIER (Non-Sterile)
TW: "恩艾萬"耳鼻喉光纖光源及載具 (未滅菌)
Taiwan·Risk Class 1·MD·M.I.ONE CO., LTD·Registered Jan 14, 2015 – Jan 14, 2025ExpiredRegistration details
- Analysis ID
- bd5406cd99c4f614aae522e60001c7bf
- License Form
- Ministry of Health Medical Device Import No. 014851
- Customs Code
- DHA09401485109
Company information
- Manufacturer
- M.I.ONE CO., LTD
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- WHOLE WELL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Fiber Optic Light Source and Vehicle (G.4350)".
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G4350 ENT fiber optic light source and vehicle
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 14, 2015
- Expiry Date
- Jan 14, 2025
About this record
Access comprehensive regulatory information for "M.I.ONE" EAR, NOSE, AND THROAT FIBEROPTIC LIGHT SOURCE AND CARRIER (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 bd5406cd99c4f614aae522e60001c7bf and manufactured by M.I.ONE CO., LTD. The authorized representative in Taiwan is WHOLE WELL CO., LTD..
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