Taiwan FDA registration 314a23151007c59b2e2c3e5ef831c0f2
“TAKAGI” Contrast Glaretester (Non-Sterile)
TW: “高木精工”對比眩光測試儀 (未滅菌)
Taiwan·Risk Class 1·MD·TAKAGI SEIKO CO., LTD.·Registered Oct 08, 2014 – Oct 08, 2024CancelledRegistration details
- Analysis ID
- 314a23151007c59b2e2c3e5ef831c0f2
- License Form
- Ministry of Health Medical Device Import No. 014554
- Customs Code
- DHA09401455403
Company information
- Manufacturer
- TAKAGI SEIKO CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- IKI MEDICAL CO., LTD.
Product details
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1460 stereo sensor
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 08, 2014
- Expiry Date
- Oct 08, 2024
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for “TAKAGI” Contrast Glaretester (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 314a23151007c59b2e2c3e5ef831c0f2 and manufactured by TAKAGI SEIKO CO., LTD.. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
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