Taiwan FDA registration 9a8c6699961398247c8aadfbff406262
"MEGA" Ear, nose and throat examination and treatment unit (Non-Sterile)
TW: "美佳" 耳鼻喉檢查及治療儀 (未滅菌)
Taiwan·Risk Class 1·MD·MEGA MEDICAL CO., LTD·Registered Mar 23, 2017 – Mar 23, 2022ExpiredRegistration details
- Analysis ID
- 9a8c6699961398247c8aadfbff406262
- License Form
- Ministry of Health Medical Device Import No. 017636
- Customs Code
- DHA09401763607
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 of identification scope of the Measures for the Administration of Medical Devices "ENT Examination and Treatment Unit (G.5300)".
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G5300 ENT Examination and Treatment Unit
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 23, 2017
- Expiry Date
- Mar 23, 2022
About this record
Access comprehensive regulatory information for "MEGA" Ear, nose and throat examination and treatment unit (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 9a8c6699961398247c8aadfbff406262 and manufactured by MEGA MEDICAL CO., LTD. The authorized representative in Taiwan is MEDWAY BME CORPORATION.
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