Taiwan FDA registration 788699ecb76fa6373197f8acd0e779c8
"Waters" Manual Eye Surgery Instruments (Sterilized)
TW: "沃特斯" 手動式眼科手術器械 (滅菌)
Taiwan·Risk Class 1·VORTEX SURGICAL·Registered Nov 06, 2020 – Nov 06, 2025ExpiredRegistration details
- Analysis ID
- 788699ecb76fa6373197f8acd0e779c8
- Customs Code
- DHA09402208809
Company information
- Manufacturer
- VORTEX SURGICAL
- Manufacturer Country
- United States
- Authorized Representative
- CONEYE 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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Nov 06, 2020
- Expiry Date
- Nov 06, 2025
About this record
Access comprehensive regulatory information for "Waters" Manual Eye Surgery Instruments (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 788699ecb76fa6373197f8acd0e779c8 and manufactured by VORTEX SURGICAL. The authorized representative in Taiwan is CONEYE CO., LTD.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices