Taiwan FDA registration 388f98bf0e7e608a635304d176969967
"Stephen" manual eye surgery instruments (unsterilized)
TW: "史帝芬"手動式眼科手術器械(未滅菌)
Taiwan·Risk Class 1·STEPHENS INSTRUMENTS·Registered Apr 14, 2006 – Apr 14, 2026ExpiredRegistration details
- Analysis ID
- 388f98bf0e7e608a635304d176969967
- Customs Code
- DHA04400386503
Company information
- Manufacturer
- STEPHENS INSTRUMENTS
- Manufacturer Country
- United States
- Authorized Representative
- BIO-LIFE 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
- Apr 14, 2006
- Expiry Date
- Apr 14, 2026
About this record
Access comprehensive regulatory information for "Stephen" manual eye surgery 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 388f98bf0e7e608a635304d176969967 and manufactured by STEPHENS INSTRUMENTS. The authorized representative in Taiwan is BIO-LIFE ENTERPRISE CO., LTD..
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