Taiwan FDA registration e8f8c8799584bec21f22a676f1275475

ZEISS Eye Refractive Machine (Unsterilized)

TW: 蔡司 眼科驗光機 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·CARL ZEISS MEDITEC AG·Registered Oct 01, 2021 – Oct 31, 2024Expired
Registration details
Analysis ID
e8f8c8799584bec21f22a676f1275475
Customs Code
DHA08401453200
Company information
Manufacturer Country
Germany
Authorized Representative
TAIWAN INSTRUMENT CO., LTD.
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
Input;; QMS/QSD
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2024
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About this record

Access comprehensive regulatory information for ZEISS Eye Refractive Machine (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e8f8c8799584bec21f22a676f1275475 and manufactured by CARL ZEISS MEDITEC AG. 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 CARL ZEISS MEDITEC AG, 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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