Taiwan FDA registration 9c1285aafd917ed52ea567911da960ad
"Takagi" corneal arc indicator (unsterilized)
TW: "高木" 角膜弧度儀 (未滅菌)
Taiwan·Risk Class 1·TAKAGI SEIKO CO., LTD.·Registered Jul 09, 2013 – Jul 09, 2023CancelledRegistration details
- Analysis ID
- 9c1285aafd917ed52ea567911da960ad
- Customs Code
- DHA04401319200
Company information
- Manufacturer
- TAKAGI SEIKO CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- TAIWAN OPTICAL CO., LTD.
Product details
- 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 Ophthalmology
- Product Type (Level 2)
- M.1350 Coratoscope
- Import Information
- import
Dates and status
- Registration Date
- Jul 09, 2013
- Expiry Date
- Jul 09, 2023
- Cancellation Date
- Sep 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "Takagi" corneal arc indicator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9c1285aafd917ed52ea567911da960ad 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. 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