Taiwan FDA registration ec502e1d79687456456e5a7fcd8e373a
"Antec" Surgical Magnifier & Accessories (Unkilled)
TW: “安泰克” 手術放大鏡及其附件 (未滅菌)
Taiwan·Risk Class 1·WENZHOU AMTECH MEDICAL TECHNOLOGY CO.,LTD·Registered Nov 28, 2024 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- ec502e1d79687456456e5a7fcd8e373a
- Customs Code
- DHA086A0019706
Company information
- Manufacturer
- WENZHOU AMTECH MEDICAL TECHNOLOGY CO.,LTD
- Manufacturer Country
- China
- Authorized Representative
- EUROTIDE TECHNOLOGY CO., LTD.
Product details
- Intended Use
- Limited to the first level of identification scope of medical equipment classification and hierarchical management, ophthalmic surgical glasses (magnifying glasses) (M.4770).
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4770 Ophthalmic surgical lenses (magnifying lenses)
- Import Information
- import
Dates and status
- Registration Date
- Nov 28, 2024
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for "Antec" Surgical Magnifier & Accessories (Unkilled) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ec502e1d79687456456e5a7fcd8e373a and manufactured by WENZHOU AMTECH MEDICAL TECHNOLOGY CO.,LTD. The authorized representative in Taiwan is EUROTIDE TECHNOLOGY CO., LTD..
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