Taiwan FDA registration ae49a3aaaff5eaa8629856c7521d28c3
"Meijia" otoscope (unsterilized)
TW: "美佳"耳鏡(未滅菌)
Taiwan·Risk Class 1·MEGA MEDICAL·Registered Dec 20, 2011 – Dec 20, 2021CancelledRegistration details
- Analysis ID
- ae49a3aaaff5eaa8629856c7521d28c3
- Customs Code
- DHA04401120101
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 range of the Measures for the Administration of Medical Devices "Otoscope (G.4770)".
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.4770 Ear Mirrors
- Import Information
- import
Dates and status
- Registration Date
- Dec 20, 2011
- Expiry Date
- Dec 20, 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" otoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ae49a3aaaff5eaa8629856c7521d28c3 and manufactured by MEGA MEDICAL. The authorized representative in Taiwan is MEDWAY BME CORPORATION.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices