Taiwan FDA registration fc00b2d21a37768d2b9e378af258d81e
Nidek corneal lamellar knife (unsterilized)
TW: 尼德克角膜板層刀(未滅菌)
Taiwan·Risk Class 1·NIDEK CO., LTD.·Registered Mar 08, 2006 – Mar 08, 2011CancelledRegistration details
- Analysis ID
- fc00b2d21a37768d2b9e378af258d81e
- Customs Code
- DHA04400283706
Company information
- Manufacturer
- NIDEK CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- IKI MEDICAL CO., LTD.
Product details
- Intended Use
- A keratoblade is an alternating current or battery-powered device used to trim tissues during corneal lamellar transplantation (cornea of partial thickness).
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4370 Corneal knife
- Import Information
- import
Dates and status
- Registration Date
- Mar 08, 2006
- Expiry Date
- Mar 08, 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 lamellar knife (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fc00b2d21a37768d2b9e378af258d81e and manufactured by NIDEK CO., LTD.. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
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