"Herriken" Manual Eye Surgery Instruments (Sterilization)
Taiwan·Risk Class 1·HURRICANE MEDICAL·Registered Jul 10, 2024 – Jul 10, 2029Active- Analysis ID
- 7567cb67ca75063d2d2350c898228480
- Customs Code
- DHA09402353309
- Manufacturer
- HURRICANE MEDICAL
- Manufacturer Country
- United States
- Authorized Representative
- BIOMEGA INSTRUMENT CO., LTD.
- Intended Use
- It is limited to the first level of identification of the "Manual Ophthalmic Surgical Instruments (M.4350)" of the Administrative Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4350 手動式眼科手術器械
- Import Information
- QMS/QSD;; 輸入
- Registration Date
- Jul 10, 2024
- Expiry Date
- Jul 10, 2029
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Access comprehensive regulatory information for "Herriken" 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 7567cb67ca75063d2d2350c898228480 and manufactured by HURRICANE MEDICAL. The authorized representative in Taiwan is BIOMEGA INSTRUMENT CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HURRICANE MEDICAL, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.