Taiwan FDA registration 2bee5703b0fe7ee3a46ea2e693054e35
"Keeler" Magnification Loupes and accessories(Non-Sterile)
TW: "凱樂" 手術放大鏡及附件(未滅菌)
Taiwan·Risk Class 1·MD·KEELER LTD.·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- 2bee5703b0fe7ee3a46ea2e693054e35
- License Form
- Ministry of Health Medical Device Import Registration No. 003280
- Customs Code
- DHA08400328001
Company information
- Manufacturer
- KEELER LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- TAIWAN OPTICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices (Ophthalmic Surgical Glasses [M.4770]).
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M4770 Ophthalmic surgical glasses (magnifying glasses)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
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 2bee5703b0fe7ee3a46ea2e693054e35 and manufactured by KEELER LTD.. The authorized representative in Taiwan is TAIWAN OPTICAL CO., LTD..
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