ZEISS Medical Corneal Mapper System (Unsterilized)
- Analysis ID
- 39b3d65baad134508887d6e3ab1404b8
- Customs Code
- DHA09401952304
- Manufacturer Country
- United States;;Singapore
- Authorized Representative
- Carl Zeiss Co., Ltd. Taipei Branch
- 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
- Input;; Contract manufacturing
- Registration Date
- Aug 21, 2018
- Expiry Date
- Aug 21, 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 Medical 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 39b3d65baad134508887d6e3ab1404b8 and manufactured by Carl Zeiss Meditec, Inc.;; Flextronics manufacturing (Singapore) Pte Ltd. The authorized representative in Taiwan is Carl Zeiss Co., Ltd. Taipei Branch.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Carl Zeiss Meditec, Inc.;; Flextronics manufacturing (Singapore) Pte Ltd, 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.