Taiwan FDA registration d1ae44631b03080c54df112a9d59a358

Eyepower Forerunner Aberration Analyzer (Unsterilized)

TW: “眼力健”前導波像差分析儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·AMO MANUFACTURING USA, LLC.·Registered Jan 24, 2013 – Jan 24, 2018Cancelled
Registration details
Analysis ID
d1ae44631b03080c54df112a9d59a358
Customs Code
DHA04401263401
Company information
Manufacturer Country
United States
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
QMS/QSD;; 輸入
Dates and status
Registration Date
Jan 24, 2013
Expiry Date
Jan 24, 2018
Cancellation Date
Dec 20, 2019
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for Eyepower Forerunner Aberration Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d1ae44631b03080c54df112a9d59a358 and manufactured by AMO MANUFACTURING USA, LLC.. The authorized representative in Taiwan is AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including AMO MANUFACTURING USA, LLC., and 2 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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