Taiwan FDA registration 32e6196c6622ff74ce5ab8e007b1b6c9

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 Sep 25, 2008 – Sep 25, 2023Cancelled
Registration details
Analysis ID
32e6196c6622ff74ce5ab8e007b1b6c9
Customs Code
DHA04400709704
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
Sep 25, 2008
Expiry Date
Sep 25, 2023
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 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 32e6196c6622ff74ce5ab8e007b1b6c9 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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