Taiwan FDA registration f95fff3df8d273d68aad06d088ba6b30
"Meijia" surgical headlamp (unsterilized)
TW: "美佳"手術用頭燈(未滅菌)
Taiwan·Risk Class 1·MEGA MEDICAL·Registered Feb 18, 2013 – Feb 18, 2018CancelledRegistration details
- Analysis ID
- f95fff3df8d273d68aad06d088ba6b30
- Customs Code
- DHA04401270702
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 "Surgical Headlamps (M.4335)".
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4335 Headlamps for surgery
- Import Information
- import
Dates and status
- Registration Date
- Feb 18, 2013
- Expiry Date
- Feb 18, 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" surgical headlamp (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f95fff3df8d273d68aad06d088ba6b30 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