Taiwan FDA registration 1e62c2e79bab5d6124697946c1836ff2
"Dell" Manual Eye Surgery Instruments (Sterilized)
TW: "戴爾" 手動式眼科手術器械 (滅菌)
Taiwan·Risk Class 1·DIAMATRIX LTD·Registered Sep 17, 2018 – Sep 17, 2028ActiveRegistration details
- Analysis ID
- 1e62c2e79bab5d6124697946c1836ff2
- Customs Code
- DHA09401961101
Company information
- Manufacturer
- DIAMATRIX LTD
- 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
- Sep 17, 2018
- Expiry Date
- Sep 17, 2028
About this record
Access comprehensive regulatory information for "Dell" 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 1e62c2e79bab5d6124697946c1836ff2 and manufactured by DIAMATRIX LTD. 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