Taiwan FDA registration 3c7d66e07a0403e8b878d6c39be453fb
"Emedica" eye surgical perfusion device (unsterilized)
TW: “艾美迪卡”眼睛手術灌注裝置 (未滅菌)
Taiwan·Risk Class 1·I-MEDICAL OPHTHALMIC INTERNATIONAL GMBH·Registered Jan 05, 2011 – Jan 05, 2026ExpiredRegistration details
- Analysis ID
- 3c7d66e07a0403e8b878d6c39be453fb
- Customs Code
- DHA04400977009
Company information
- Manufacturer
- I-MEDICAL OPHTHALMIC INTERNATIONAL GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- RAY HUNG INSTRUMENT CO., LTD.
Product details
- Intended Use
- It is limited to the first level identification scope of ophthalmic surgical perfusion devices (M.4360) in the classification and grading management measures for medical devices.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4360 Perfusion device for ophthalmic surgery
- Import Information
- import
Dates and status
- Registration Date
- Jan 05, 2011
- Expiry Date
- Jan 05, 2026
About this record
Access comprehensive regulatory information for "Emedica" eye surgical perfusion device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3c7d66e07a0403e8b878d6c39be453fb and manufactured by I-MEDICAL OPHTHALMIC INTERNATIONAL GMBH. The authorized representative in Taiwan is RAY HUNG INSTRUMENT CO., LTD..
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