Taiwan FDA registration ea53868a44ad6e5e652a6416834fa1cd
Alcon Manual Eye Surgery Instruments (Sterilization)
TW: “愛爾康”手動式眼科手術器械 (滅菌)
Taiwan·Risk Class 1·ALCON MANUFACTURING, LTD.·Registered Jun 16, 2006 – Jun 16, 2011CancelledRegistration details
- Analysis ID
- ea53868a44ad6e5e652a6416834fa1cd
- Customs Code
- DHA04400472505
Company information
- Manufacturer
- ALCON MANUFACTURING, LTD.
- 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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jun 16, 2006
- Expiry Date
- Jun 16, 2011
- Cancellation Date
- Nov 19, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Alcon Manual Eye Surgery Instruments (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ea53868a44ad6e5e652a6416834fa1cd and manufactured by ALCON MANUFACTURING, LTD.. The authorized representative in Taiwan is ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND).
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