"Keeler" Magnification Loupes and accessories (Non-Sterile)
Taiwan·Risk Class 1·MD·Keeler Limited·Registered Jan 29, 2015 – Jan 29, 2025Cancelled- Analysis ID
- 26e1d2c64f91a01795a0cf41a805615d
- License Form
- Ministry of Health Medical Device Import No. 014884
- Customs Code
- DHA09401488401
- Manufacturer
- Keeler Limited
- Manufacturer Country
- United Kingdom
- Authorized Representative
- EVERLIGHT INSTRUMENT CO., LTD.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M4770 Ophthalmic surgical glasses (magnifying glasses)
- Import Information
- Imported from abroad
- Registration Date
- Jan 29, 2015
- Expiry Date
- Jan 29, 2025
- Status
- Logged out
- Reason
- 轉為登錄字號
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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 26e1d2c64f91a01795a0cf41a805615d 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.