Taiwan FDA registration 3da0f36cf6861b5166c9400c184d2410
"Aitker" Manual Eye Surgery Instruments (Sterilized)
TW: "艾特克" 手動式眼科手術器械 (滅菌)
Taiwan·Risk Class 1·EYE TECHNOLOGY LTD·Registered Mar 03, 2016 – Mar 03, 2021CancelledRegistration details
- Analysis ID
- 3da0f36cf6861b5166c9400c184d2410
- Customs Code
- DHA09401622000
Company information
- Manufacturer
- EYE TECHNOLOGY LTD
- Manufacturer Country
- United Kingdom
- Authorized Representative
- CONEYE CO., LTD
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
- Mar 03, 2016
- Expiry Date
- Mar 03, 2021
- Cancellation Date
- Oct 06, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Aitker" Manual Eye Surgery Instruments (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3da0f36cf6861b5166c9400c184d2410 and manufactured by EYE TECHNOLOGY LTD. The authorized representative in Taiwan is CONEYE CO., LTD.
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