Taiwan FDA registration eca44ebf33b4cc112f71452897073b2e

"Medmont" Acuity Tester (Non-Sterile)

TW: "梅德蒙" 視功能檢測軟體 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·MEDMONT INTERNATIONAL PTY LTD·Registered Jul 12, 2016 – Jul 12, 2021Expired
Registration details
Analysis ID
eca44ebf33b4cc112f71452897073b2e
License Form
Ministry of Health Medical Device Import No. 016765
Customs Code
DHA09401676500
Company information
Manufacturer Country
Australia
Authorized Representative
IKI MEDICAL CO., LTD.
Product details
Intended Use
Limited to the first level recognition range of ophthalmic projectors (M.1680) for the management of medical equipment.
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M1680 Ophthalmic Projector
Import Information
Imported from abroad
Dates and status
Registration Date
Jul 12, 2016
Expiry Date
Jul 12, 2021
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About this record

Access comprehensive regulatory information for "Medmont" Acuity Tester (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number eca44ebf33b4cc112f71452897073b2e and manufactured by MEDMONT INTERNATIONAL PTY LTD. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MEDMONT INTERNATIONAL PTY LTD, 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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