Taiwan FDA registration 8d051417dd5cd221a0148afbbeeac4ef
"Bausch & Len" Ophthalmic Manual Device (Unsterilized)
TW: “博士倫”視導眼科手動式器械(未滅菌)
Taiwan·Risk Class 1·BAUSCH & LOMB GMBH·Registered Jan 11, 2007 – Jan 11, 2027ActiveRegistration details
- Analysis ID
- 8d051417dd5cd221a0148afbbeeac4ef
- Customs Code
- DHA04400552005
Company information
- Manufacturer
- BAUSCH & LOMB GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- BAUSCH & LOMB TAIWAN LIMITED
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
- Jan 11, 2007
- Expiry Date
- Jan 11, 2027
About this record
Access comprehensive regulatory information for "Bausch & Len" Ophthalmic Manual Device (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8d051417dd5cd221a0148afbbeeac4ef and manufactured by BAUSCH & LOMB GMBH. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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