Taiwan FDA registration 58c4586a51ce13814fb8938d0cbd345f
"Siji" manual eye surgery instruments (sterilization)
TW: “思吉”手動式眼科手術器械（滅菌）
Taiwan·Risk Class 1·SURGICAL SPECIALTIES CORPORATION·Registered Oct 02, 2009 – Oct 02, 2019CancelledRegistration details
- Analysis ID
- 58c4586a51ce13814fb8938d0cbd345f
- Customs Code
- DHA04400817605
Company information
- Manufacturer
- SURGICAL SPECIALTIES CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- CLINICO INC.
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
- Oct 02, 2009
- Expiry Date
- Oct 02, 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 "Siji" 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 58c4586a51ce13814fb8938d0cbd345f and manufactured by SURGICAL SPECIALTIES CORPORATION. The authorized representative in Taiwan is CLINICO INC..
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