Taiwan FDA registration 632ace8fbff5eb3fe757d917225e6e2f

"ZEISS" automatic refractometer (unsterilized)

TW: "蔡司" 自動驗光機 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·VISIONIX LTD;; Carl Zeiss Vision GmbH·Registered Oct 01, 2021 – Oct 31, 2026Active
Registration details
Analysis ID
632ace8fbff5eb3fe757d917225e6e2f
Customs Code
DHA08401673508
Company information
Manufacturer Country
Israel;;Germany
Authorized Representative
Carl Zeiss Co., Ltd. Taipei Branch
Product details
Intended Use
Limited to the first level identification scope of the "Automatic Ophthalmic Refractive Machine (M.1760)" of the Measures for the Classification and Grading of Medical Equipment.
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.1760 Automatic Ophthalmic Optical Machine
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2026
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About this record

Access comprehensive regulatory information for "ZEISS" automatic refractometer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 632ace8fbff5eb3fe757d917225e6e2f and manufactured by VISIONIX LTD;; Carl Zeiss Vision GmbH. 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 VISION GMBH;; Made (部分製程) in ISRAEL, 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.

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