Taiwan FDA registration cfec2705f00e17052d25183c090f10cf
"ZEISS" VISUSCREEN Ophthalmic Projector (non-sterile)
TW: "蔡司" 視標投影機 (未滅菌)
Taiwan·Risk Class 1·MD·CARL ZEISS VISION GMBH·Registered Mar 26, 2015 – Mar 26, 2020CancelledRegistration details
- Analysis ID
- cfec2705f00e17052d25183c090f10cf
- License Form
- Ministry of Health Medical Device Import No. 015052
- Customs Code
- DHA09401505200
Company information
- Manufacturer
- CARL ZEISS VISION GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Yakili Corporation of Agili
Product details
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1680 Ophthalmic Projector
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 26, 2015
- Expiry Date
- Mar 26, 2020
- Cancellation Date
- Jan 31, 2019
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "ZEISS" VISUSCREEN Ophthalmic Projector (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 cfec2705f00e17052d25183c090f10cf and manufactured by CARL ZEISS VISION GMBH. The authorized representative in Taiwan is Yakili Corporation of Agili.
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