Taiwan FDA registration 3f73e77c740533dc39c69aa8159758c6
Rodensid ophthalmic projector (unsterilized)
TW: “羅敦司得”眼科用投影機 (未滅菌)
Taiwan·Risk Class 1·RODENSTOCK INSTRUMENTE (TOMEY GMBH)·Registered Jun 21, 2013 – Jun 21, 2018CancelledRegistration details
- Analysis ID
- 3f73e77c740533dc39c69aa8159758c6
- Customs Code
- DHA04401312801
Company information
- Manufacturer
- RODENSTOCK INSTRUMENTE (TOMEY GMBH)
- Manufacturer Country
- Germany
- Authorized Representative
- JECKSEN CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of ophthalmic projectors (M.1680) for the management of medical equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1680 眼科用投影機
- Import Information
- import
Dates and status
- Registration Date
- Jun 21, 2013
- Expiry Date
- Jun 21, 2018
- Cancellation Date
- Nov 21, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Rodensid ophthalmic projector (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3f73e77c740533dc39c69aa8159758c6 and manufactured by RODENSTOCK INSTRUMENTE (TOMEY GMBH). The authorized representative in Taiwan is JECKSEN CO., LTD..
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