Taiwan FDA registration 45a963fa94fbf31a243a6e13816614c8
"Zeiss" optical interferometric anterior chamber tomography
TW: "蔡司"光學干涉眼前房斷層掃描儀
Taiwan·Risk Class 2·CARL ZEISS MEDITEC, INC.·Registered Dec 12, 2006 – Dec 12, 2021CancelledRegistration details
- Analysis ID
- 45a963fa94fbf31a243a6e13816614c8
- Customs Code
- DHA00601748601
Company information
- Manufacturer
- CARL ZEISS MEDITEC, INC.
- Manufacturer Country
- United States
- Authorized Representative
- TAIWAN INSTRUMENT CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1570 Fundus Mirrors
- Import Information
- import
Dates and status
- Registration Date
- Dec 12, 2006
- Expiry Date
- Dec 12, 2021
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Zeiss" optical interferometric anterior chamber tomography in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 45a963fa94fbf31a243a6e13816614c8 and manufactured by CARL ZEISS MEDITEC, INC.. The authorized representative in Taiwan is TAIWAN INSTRUMENT CO., LTD..
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