Taiwan FDA registration 7404093426669deb1bf2467ac42eb645
"SIDAPHARM" Manual Ophthalmic Surgical Instrument (Sterile)
TW: "賽達方" 手動式眼科手術器械 (滅菌)
Taiwan·Risk Class 1·MD·SIDAPHARM P.C.·Registered Jul 27, 2018 – Jul 27, 2023ExpiredRegistration details
- Analysis ID
- 7404093426669deb1bf2467ac42eb645
- License Form
- Ministry of Health Medical Device Import No. 019422
- Customs Code
- DHA09401942201
Company information
- Manufacturer
- SIDAPHARM P.C.
- Manufacturer Country
- Greece
- Authorized Representative
- EVERLIGHT INSTRUMENT 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 Ophthalmic devices
- Product Type (Level 2)
- M4350 Manual Ophthalmic Surgery Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 27, 2018
- Expiry Date
- Jul 27, 2023
About this record
Access comprehensive regulatory information for "SIDAPHARM" Manual Ophthalmic Surgical Instrument (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7404093426669deb1bf2467ac42eb645 and manufactured by SIDAPHARM P.C.. The authorized representative in Taiwan is EVERLIGHT INSTRUMENT CO., LTD..
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