Taiwan FDA registration 9d1a8142aeae67ec26c59c2f50b2386a
"Nidek" corneal curvature
TW: "尼德克" 角膜弧度儀
Taiwan·Risk Class 1·NIDEK CO., LTD.·Registered Feb 22, 2006 – Feb 22, 2011CancelledRegistration details
- Analysis ID
- 9d1a8142aeae67ec26c59c2f50b2386a
- Customs Code
- DHA04400269502
Company information
- Manufacturer
- NIDEK CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- IKI MEDICAL CO., LTD.
Product details
- Intended Use
- It is an alternating current or battery-powered device used to measure and evaluate the curvature of the cornea of the eye. The lines and circles in the keratometer are used to observe the corneal reflex. The general type of device includes a photokeratometer, which can be used to record the curvature of the cornea using corneal photography.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1350 Coratoscope
- Import Information
- import
Dates and status
- Registration Date
- Feb 22, 2006
- Expiry Date
- Feb 22, 2011
- Cancellation Date
- Jan 21, 2013
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Nidek" corneal curvature in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9d1a8142aeae67ec26c59c2f50b2386a and manufactured by NIDEK CO., LTD.. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
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