Taiwan FDA registration a1b1403e5ace2a924211ae7edf834bc4

"Meida" ophthalmic keratoscope (unsterilized)

TW: “美達”眼科角膜鏡 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MEDA CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
a1b1403e5ace2a924211ae7edf834bc4
Customs Code
DHA08600092101
Company information
Manufacturer
MEDA CO., LTD.
Manufacturer Country
China
Authorized Representative
JUN FENG OPTICAL CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of the "corneoscopy (M.1350)" of the classification and grading management method for medical equipment.
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.1350 Coratoscope
Import Information
Input;; Chinese goods
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2025
Companies making similar products

Top companies providing products similar to ""Meida" ophthalmic keratoscope (unsterilized)"

Recent registrations

Recently registered similar products

About this record

Access comprehensive regulatory information for "Meida" ophthalmic keratoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a1b1403e5ace2a924211ae7edf834bc4 and manufactured by MEDA CO., LTD.. The authorized representative in Taiwan is JUN FENG OPTICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MEDA CO., 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.

Free DatabasePowered by Pure Global AI89,000+ Devices1 Competitors1 Recent Registrations