Taiwan FDA registration 9b4d8e87aec19201886b3b812cea8246
"Mei Shiai" manual ophthalmic surgical instruments (unsterilized)
TW: “梅適艾”手動式眼科手術器械（未滅菌）
Taiwan·Risk Class 1·MSI PRECISION SPECIALTY INSTRUMENTS·Registered Sep 13, 2010 – Sep 13, 2025ExpiredRegistration details
- Analysis ID
- 9b4d8e87aec19201886b3b812cea8246
- Customs Code
- DHA04400919106
Company information
- Manufacturer
- MSI PRECISION SPECIALTY INSTRUMENTS
- Manufacturer Country
- United States
- Authorized Representative
- TAIWAN HWA IN ENTERPRISE 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 13, 2010
- Expiry Date
- Sep 13, 2025
About this record
Access comprehensive regulatory information for "Mei Shiai" manual ophthalmic surgical instruments (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9b4d8e87aec19201886b3b812cea8246 and manufactured by MSI PRECISION SPECIALTY INSTRUMENTS. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..
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