"Takagi" Keratometer (Non-Sterile)
Taiwan·Risk Class 1·MD·TAKAGI SEIKO CO., LTD.·Registered Dec 07, 2015 – Dec 07, 2020Cancelled- Analysis ID
- 3adfec006e75ef774441fcacc1962ed5
- License Form
- Ministry of Health Medical Device Import No. 015941
- Customs Code
- DHA09401594102
- Manufacturer
- TAKAGI SEIKO CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- IKI MEDICAL CO., LTD.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1350 Keatoscope
- Import Information
- Imported from abroad
- Registration Date
- Dec 07, 2015
- Expiry Date
- Dec 07, 2020
- Cancellation Date
- Aug 05, 2022
- Status
- Logged out
- Reason
- 未展延而逾期者
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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 3adfec006e75ef774441fcacc1962ed5 and manufactured by TAKAGI SEIKO CO., LTD.. The authorized representative in Taiwan is IKI MEDICAL 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.