Taiwan FDA registration 85e90adbf8e374e7fc045d197baf1736
"Esco" manual eye surgery instruments (unsterilized)
TW: “愛斯可”手動式眼科手術器械 (未滅菌)
Taiwan·Risk Class 1·ASICO LLC·Registered Nov 30, 2007 – Nov 30, 2022CancelledRegistration details
- Analysis ID
- 85e90adbf8e374e7fc045d197baf1736
- Customs Code
- DHA04400634301
Company information
- Manufacturer
- ASICO LLC
- Manufacturer Country
- United States
- Authorized Representative
- ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND)
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Eye Surgery Instruments (M.4350)".
- 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 30, 2007
- Expiry Date
- Nov 30, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Esco" 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 85e90adbf8e374e7fc045d197baf1736 and manufactured by ASICO LLC. The authorized representative in Taiwan is ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND).
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