Taiwan FDA registration 6029101d5858e9cc5710a88653e3fa25
"Osco" Ophthalmic Manual Device (Unsterilized)
TW: “歐斯科”眼科手動式器械 (未滅菌)
Taiwan·Risk Class 1·ASICO LLC·Registered Jun 11, 2009 – Jun 11, 2024ExpiredRegistration details
- Analysis ID
- 6029101d5858e9cc5710a88653e3fa25
- Customs Code
- DHA04400781702
Company information
- Manufacturer
- ASICO LLC
- Manufacturer Country
- United States
- Authorized Representative
- SHIN SHENG PHARMACEUTICAL 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
- Jun 11, 2009
- Expiry Date
- Jun 11, 2024
About this record
Access comprehensive regulatory information for "Osco" 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 6029101d5858e9cc5710a88653e3fa25 and manufactured by ASICO LLC. The authorized representative in Taiwan is SHIN SHENG PHARMACEUTICAL 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