"Keeler" Magnification Loupes and accessories (Non-Sterile)
Taiwan·Risk Class 1·MD·Keeler Limited·Registered Oct 01, 2021 – Oct 31, 2025Expired- Analysis ID
- 83c54b82ddc93a36e7c17ca1947375fc
- License Form
- Ministry of Health Medical Device Import Registration No. 014884
- Customs Code
- DHA08401488402
- Manufacturer
- Keeler Limited
- Manufacturer Country
- United Kingdom
- Authorized Representative
- EVERLIGHT INSTRUMENT CO., LTD.
- Intended Use
- Limited to the first level of identification scope of "Ophthalmic Surgical Glasses (Magnifying Glasses) (M.4770)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M4770 Ophthalmic surgical glasses (magnifying glasses)
- Import Information
- Imported from abroad
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
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Access comprehensive regulatory information for "Keeler" Magnification Loupes and accessories (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 83c54b82ddc93a36e7c17ca1947375fc and manufactured by Keeler Limited. The authorized representative in Taiwan is EVERLIGHT INSTRUMENT CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Keeler Limited, 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.