Taiwan FDA registration 38b1b228c5a0657c2f6cc2d667172985
"Meijia" ENT Examination and Treatment Device (Unsterilized)
TW: 〝美佳〞耳鼻喉檢查及治療儀 (未滅菌)
Taiwan·Risk Class 1·MEGA MEDICAL CO., LTD·Registered Mar 28, 2006 – Mar 28, 2021CancelledRegistration details
- Analysis ID
- 38b1b228c5a0657c2f6cc2d667172985
- Customs Code
- DHA04400322608
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 range of the Measures for the Administration of Medical Devices (ENT Examination and Treatment Table [G.5300]).
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.5300 ENT examination and treatment table
- Import Information
- import
Dates and status
- Registration Date
- Mar 28, 2006
- Expiry Date
- Mar 28, 2021
- Cancellation Date
- Aug 28, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Meijia" ENT Examination and Treatment Device (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 38b1b228c5a0657c2f6cc2d667172985 and manufactured by MEGA MEDICAL CO., LTD. The authorized representative in Taiwan is MEDWAY BME CORPORATION.
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