Taiwan FDA registration 9271182f13e75f5ef3f0e10386ac0dbc
"Orthogonal" manual ophthalmic surgery instrument (unsterile)
TW: "正通" 手動式眼科手術器械 (未滅菌)
Taiwan·Risk Class 1·SUQIAN ZHENGTONG MEDICAL INSTRUMENT CO., LTD.·Registered Jan 30, 2015 – Jan 30, 2020CancelledRegistration details
- Analysis ID
- 9271182f13e75f5ef3f0e10386ac0dbc
- Customs Code
- DHA09600232402
Company information
- Manufacturer
- SUQIAN ZHENGTONG MEDICAL INSTRUMENT 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
- Input;; Chinese goods
Dates and status
- Registration Date
- Jan 30, 2015
- Expiry Date
- Jan 30, 2020
- 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 "Orthogonal" manual ophthalmic surgery instrument (unsterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9271182f13e75f5ef3f0e10386ac0dbc and manufactured by SUQIAN ZHENGTONG MEDICAL INSTRUMENT CO., LTD.. The authorized representative in Taiwan is SHENG SHIUAN INDUSTRIAL CO., LTD..
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