Taiwan FDA registration 67e003c109ee3d0241309b60bdb6cb84

Guobo corneal mapper (unsterilized)

TW: 鷗博角膜地圖儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Eagle Vision Co., Ltd. Shilin Factory·Registered Jan 15, 2014 – Jan 15, 2024Cancelled
Registration details
Analysis ID
67e003c109ee3d0241309b60bdb6cb84
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
VISION TECHNOLOGY CO., LTD.
Product details
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
Domestic
Dates and status
Registration Date
Jan 15, 2014
Expiry Date
Jan 15, 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 Guobo corneal mapper (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 67e003c109ee3d0241309b60bdb6cb84 and manufactured by Eagle Vision Co., Ltd. Shilin Factory. The authorized representative in Taiwan is VISION TECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Eagle Vision Co., Ltd. Shilin Factory, 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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