Taiwan FDA registration c0a9a2af4c5393b22e5cc7aa67ce8ea8
"Meijia" ENT Fiber Optic Light Source and Vehicle (Unsterilized)
TW: "美佳" 耳鼻喉光纖光源及載具 (未滅菌)
Taiwan·Risk Class 1·MEGA MEDICAL·Registered Jan 29, 2013 – Jan 29, 2018CancelledRegistration details
- Analysis ID
- c0a9a2af4c5393b22e5cc7aa67ce8ea8
- Customs Code
- DHA04401264707
Company information
- Manufacturer
- MEGA MEDICAL
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- MEDWAY BME CORPORATION
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 Science
- Product Type (Level 2)
- G.4350 Ear, nose and throat optical fiber light sources and carriers
- Import Information
- import
Dates and status
- Registration Date
- Jan 29, 2013
- Expiry Date
- Jan 29, 2018
- Cancellation Date
- Nov 26, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Meijia" ENT Fiber Optic Light Source and Vehicle (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c0a9a2af4c5393b22e5cc7aa67ce8ea8 and manufactured by MEGA MEDICAL. The authorized representative in Taiwan is MEDWAY BME CORPORATION.
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