Taiwan FDA registration 172d2a40c8ead89bceddf63fbf36bd86

"Meida" ophthalmic keratoscope (unsterilized)

TW: “美達”眼科角膜鏡 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MEDA CO., LTD.·Registered May 06, 2010 – May 06, 2025Cancelled
Registration details
Analysis ID
172d2a40c8ead89bceddf63fbf36bd86
Customs Code
DHA04600092101
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 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
Chinese goods;; input
Dates and status
Registration Date
May 06, 2010
Expiry Date
May 06, 2025
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 "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 172d2a40c8ead89bceddf63fbf36bd86 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.

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