Taiwan FDA registration 763d216d399d0a24f7f170ae81c91106
"MEGA" ear, nose, and throat fiberoptic light source and carrier (Non-Sterile)
TW: "美佳" 耳鼻喉光纖光源及載具 (未滅菌)
Taiwan·Risk Class 1·MD·MEGA MEDICAL CO., LTD·Registered Apr 24, 2019 – Apr 24, 2024ExpiredRegistration details
- Analysis ID
- 763d216d399d0a24f7f170ae81c91106
- License Form
- Ministry of Health Medical Device Import No. 020361
- Customs Code
- DHA09402036104
Company information
- Manufacturer
- MEGA MEDICAL CO., LTD
- 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 device
- Product Type (Level 2)
- G4350 ENT fiber optic light source and vehicle
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 24, 2019
- Expiry Date
- Apr 24, 2024
About this record
Access comprehensive regulatory information for "MEGA" 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 763d216d399d0a24f7f170ae81c91106 and manufactured by MEGA MEDICAL CO., LTD. The authorized representative in Taiwan is MEDWAY BME CORPORATION.
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