Taiwan FDA registration 0553adcd6c00f54d7d8066719c2dd1fe
"OSCO" AII-7000 (unsterilized)
TW: "歐斯科"愛依-7000(未滅菌)
Taiwan·Risk Class 1·ASICO LLC·Registered Nov 11, 2005 – Nov 11, 2010CancelledRegistration details
- Analysis ID
- 0553adcd6c00f54d7d8066719c2dd1fe
- Customs Code
- DHA04400187904
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
- Nov 11, 2005
- Expiry Date
- Nov 11, 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-7000 (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0553adcd6c00f54d7d8066719c2dd1fe and manufactured by ASICO LLC. The authorized representative in Taiwan is WELL SHIP INDUSTRIAL CO., LTD..
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