Taiwan FDA registration d1c276d65685d383c7c1d290a63bc1f4
OTGO Magnifier and its accessories (unsterilized)
TW: 奧特戈 放大鏡及其附件 (未滅菌)
Taiwan·Risk Class 1·Optergo AB·Registered Jun 08, 2023 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- d1c276d65685d383c7c1d290a63bc1f4
- Customs Code
- DHA084a0019002
Company information
- Manufacturer
- Optergo AB
- Manufacturer Country
- Sweden
- Authorized Representative
- UNIGLIFE BIOMED CO., LTD.
Product details
- Intended Use
- Limited to the first level of classification and grading management of medical devices, "Ophthalmic surgical glasses (magnifying glasses) (M.4770)".
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4770 Ophthalmic surgical lenses (magnifying lenses)
Dates and status
- Registration Date
- Jun 08, 2023
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for OTGO Magnifier and its accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d1c276d65685d383c7c1d290a63bc1f4 and manufactured by Optergo AB. The authorized representative in Taiwan is UNIGLIFE BIOMED CO., LTD..
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices