Taiwan FDA registration f4c2a1117243fc1d3b3c2523889c91dc
"Meitei" manual ophthalmic surgery instrument (unsterilized)
TW: “美帝”手動式眼科手術器械（未滅菌）
Taiwan·Risk Class 1·AMIDIA LTD.·Registered Sep 21, 2009 – Sep 21, 2024ExpiredRegistration details
- Analysis ID
- f4c2a1117243fc1d3b3c2523889c91dc
- Customs Code
- DHA04400811702
Company information
- Manufacturer
- AMIDIA LTD.
- Manufacturer Country
- Switzerland
- Authorized Representative
- MED-TECH MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the "Manual Ophthalmic Surgical Instruments (M.4350)" of the Measures for the Classification and Grading of Medical Equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4350 手動式眼科手術器械
- Import Information
- import
Dates and status
- Registration Date
- Sep 21, 2009
- Expiry Date
- Sep 21, 2024
About this record
Access comprehensive regulatory information for "Meitei" manual ophthalmic surgery instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f4c2a1117243fc1d3b3c2523889c91dc and manufactured by AMIDIA LTD.. The authorized representative in Taiwan is MED-TECH MEDICAL CO., LTD..
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