"TAKAGI" Keratometer (Non-Sterile)
Taiwan·Risk Class 1·MD·TAKAGI SEIKO CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2023Expired- Analysis ID
- 9b9c24083f982e0f837c1bf2a4bdedaf
- License Form
- Ministry of Health Medical Device Import Registration No. 013192
- Customs Code
- DHA08401319207
- Manufacturer
- TAKAGI SEIKO CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- TAIWAN OPTICAL CO., LTD.
- Intended Use
- Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1350 Keatoscope
- Import Information
- Imported from abroad
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2023
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Access comprehensive regulatory information for "TAKAGI" Keratometer (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 9b9c24083f982e0f837c1bf2a4bdedaf and manufactured by TAKAGI SEIKO CO., LTD.. The authorized representative in Taiwan is TAIWAN OPTICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TAKAGI SEIKO CO., LTD., 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.