Taiwan FDA registration 4462c64921f0ad5781d8105517de43e0

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 Sep 24, 2014 – Sep 24, 2024Cancelled
Registration details
Analysis ID
4462c64921f0ad5781d8105517de43e0
Customs Code
DHA09401453206
Company information
Manufacturer Country
Germany
Authorized Representative
TAIWAN INSTRUMENT CO., LTD.
Product details
Intended Use
Limited to the first level recognition range of ophthalmic optometry machine (M.1760) of the management measures for 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
Sep 24, 2014
Expiry Date
Sep 24, 2024
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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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 4462c64921f0ad5781d8105517de43e0 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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