Taiwan FDA registration 6aca10c2209e055ceed15e6be2bde2cc
"Special Report" manual ophthalmic surgery instrument (unsterilized)
TW: “特申”手動式眼科手術器械 (未滅菌)
Taiwan·Risk Class 1·HUAIAN TISURG MEDICAL INSTRUMENTS CO., LTD.·Registered Dec 22, 2014 – Dec 22, 2019CancelledRegistration details
- Analysis ID
- 6aca10c2209e055ceed15e6be2bde2cc
- Customs Code
- DHA09600229100
Company information
- Manufacturer
- HUAIAN TISURG MEDICAL INSTRUMENTS CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- SHENG SHIUAN INDUSTRIAL 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
- Chinese goods;; input
Dates and status
- Registration Date
- Dec 22, 2014
- Expiry Date
- Dec 22, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Special Report" manual ophthalmic surgery instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6aca10c2209e055ceed15e6be2bde2cc and manufactured by HUAIAN TISURG MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is SHENG SHIUAN INDUSTRIAL CO., LTD..
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