ZEISS corneal mapper system (unsterilized)
Taiwan·Risk Class 1·FLEXTRONICS MANUFACTURING(SINGAPORE) PTD LTD;; CARL ZEISS MEDITEC INC.·Registered Apr 20, 2018 – Apr 20, 2023Cancelled- Analysis ID
- c8ad486d1d923081b80c0ad74a339a11
- Customs Code
- DHA09401899300
- Manufacturer Country
- United States;;Singapore
- Authorized Representative
- TAIWAN INSTRUMENT CO., LTD.
- Intended Use
- Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1350 Coratoscope
- Import Information
- Contract manufacturing;; input
- Registration Date
- Apr 20, 2018
- Expiry Date
- Apr 20, 2023
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for ZEISS corneal mapper system (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c8ad486d1d923081b80c0ad74a339a11 and manufactured by FLEXTRONICS MANUFACTURING(SINGAPORE) PTD LTD;; CARL ZEISS MEDITEC INC.. The authorized representative in Taiwan is TAIWAN INSTRUMENT CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FLEXTRONICS MANUFACTURING(SINGAPORE) PTD LTD;; CARL ZEISS MEDITEC INC., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.