Taiwan FDA registration 9b53fc5af084ab02106f0d657814d072
"OSCO" titanium ophthalmic equipment (unsterilized)
TW: "歐思科" 鈦合金眼科器材 (未滅菌)
Taiwan·Risk Class 1·ASICO LLC·Registered Oct 28, 2005 – Oct 28, 2010CancelledRegistration details
- Analysis ID
- 9b53fc5af084ab02106f0d657814d072
- Customs Code
- DHA04400142504
Company information
- Manufacturer
- ASICO LLC
- Manufacturer Country
- United States
- Authorized Representative
- WELL SHIP INDUSTRIAL CO., LTD.
Product details
- Intended Use
- Manual eye surgery instruments are non-electric, hand-held devices designed to assist or perform eye surgery.
- 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
- Oct 28, 2005
- Expiry Date
- Oct 28, 2010
- Cancellation Date
- Nov 23, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "OSCO" titanium ophthalmic equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9b53fc5af084ab02106f0d657814d072 and manufactured by ASICO LLC. The authorized representative in Taiwan is WELL SHIP INDUSTRIAL 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