Taiwan FDA registration 3dad50adf5611539e2800fc73e5b376e
"OSCO" AII-6000 Series Manual Eye Surgery Instruments (Unsterilized)
TW: "歐斯科" 愛依-6000系列手動式 眼科手術器械 (未滅菌)
Taiwan·Risk Class 1·ASICO LLC·Registered Oct 31, 2005 – Oct 31, 2010CancelledRegistration details
- Analysis ID
- 3dad50adf5611539e2800fc73e5b376e
- Customs Code
- DHA04400162805
Company information
- Manufacturer
- ASICO LLC
- Manufacturer Country
- United States
- Authorized Representative
- WELL SHIP INDUSTRIAL CO., LTD.
Product details
- Intended Use
- Non-electric, hand-held devices used 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 31, 2005
- Expiry Date
- Oct 31, 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" AII-6000 Series Manual Eye Surgery Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3dad50adf5611539e2800fc73e5b376e and manufactured by ASICO LLC. The authorized representative in Taiwan is WELL SHIP INDUSTRIAL CO., LTD..
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