Taiwan FDA registration 589e96af77b644c6ce0ff649aeaf79f9
"TAKAGI" View Tester(Non-Sterile)
TW: "高木"自覺式驗光儀(未滅菌)
Taiwan·Risk Class 1·MD·TAKAGI SEIKO CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- 589e96af77b644c6ce0ff649aeaf79f9
- License Form
- Ministry of Health Medical Device Import Registration No. 002941
- Customs Code
- DHA08400294101
Company information
- Manufacturer
- TAKAGI SEIKO CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- TAIWAN OPTICAL CO., LTD.
Product details
- Intended Use
- A manual refractometer is a group of lenses of different refractive intensities to measure refractive errors in the eye.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1770 Manual Fold Meter
- 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 "TAKAGI" View Tester(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 589e96af77b644c6ce0ff649aeaf79f9 and manufactured by TAKAGI SEIKO CO., LTD.. The authorized representative in Taiwan is TAIWAN OPTICAL CO., LTD..
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