Taiwan FDA registration 94a14c8bd254c0a6bf8dd8b63e9f5769
"ZEISS" optotype projector (unsterilized)
TW: ”蔡司”視標投影機(未滅菌)
Taiwan·Risk Class 1·CARL ZEISS VISION GMBH·Registered Mar 24, 2006 – Mar 24, 2016CancelledRegistration details
- Analysis ID
- 94a14c8bd254c0a6bf8dd8b63e9f5769
- Customs Code
- DHA04400314100
Company information
- Manufacturer
- CARL ZEISS VISION GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Yakili Corporation of Agili
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Equipment (ophthalmic projectors [M.1680]).
- 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
- Mar 24, 2006
- Expiry Date
- Mar 24, 2016
- Cancellation Date
- Nov 16, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期;;自請註銷
About this record
Access comprehensive regulatory information for "ZEISS" optotype 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 94a14c8bd254c0a6bf8dd8b63e9f5769 and manufactured by CARL ZEISS VISION GMBH. The authorized representative in Taiwan is Yakili Corporation of Agili.
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