Taiwan FDA registration bdb66fda30548a130e715e775321f886
"Vixing" keratoscope (unsterilized)
TW: "威栩靈" 角膜鏡 (未滅菌)
Taiwan·Risk Class 1·WELCH ALLYN INC.·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- bdb66fda30548a130e715e775321f886
- Customs Code
- DHA08401926502
Company information
- Manufacturer
- WELCH ALLYN INC.
- Manufacturer Country
- United States
- Authorized Representative
- BIOMEGA INSTRUMENT CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the "corneoscopy (M.1350)" of the classification and grading management method for medical equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1350 Coratoscope
- Import Information
- import
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "Vixing" keratoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bdb66fda30548a130e715e775321f886 and manufactured by WELCH ALLYN INC.. The authorized representative in Taiwan is BIOMEGA INSTRUMENT CO., LTD..
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