Taiwan FDA registration bd3b777eea1b4bf4e93631d3695b83c1
“Zeiss” i.Terminal 2 (Non-Sterile)
TW: “蔡司”瞳孔計 (未滅菌)
Taiwan·Risk Class 1·MD·CARL ZEISS VISION GMBH·Registered Aug 06, 2018 – Aug 06, 2023CancelledRegistration details
- Analysis ID
- bd3b777eea1b4bf4e93631d3695b83c1
- License Form
- Ministry of Health Medical Device Import No. 019456
- Customs Code
- DHA09401945602
Company information
- Manufacturer
- CARL ZEISS VISION GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- CARL ZEISS CO., LTD.
Product details
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1700 Pupillometer
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 06, 2018
- Expiry Date
- Aug 06, 2023
- Cancellation Date
- Sep 13, 2021
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for “Zeiss” i.Terminal 2 (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 bd3b777eea1b4bf4e93631d3695b83c1 and manufactured by CARL ZEISS VISION GMBH. The authorized representative in Taiwan is CARL ZEISS CO., LTD..
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