Taiwan FDA registration 25faa38c5fb275ccffe17883a1427a86

"Enmedia" Manual Eye Surgery Instruments (Unsterilized)

TW: "恩美帝亞" 手動式眼科手術器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·AMIDIA LTD.·Registered May 21, 2013 – May 21, 2023Expired
Registration details
Analysis ID
25faa38c5fb275ccffe17883a1427a86
Customs Code
DHA04401303405
Company information
Manufacturer
AMIDIA LTD.
Manufacturer Country
Switzerland
Authorized Representative
VISIONRISE ENTERPRISE CO., LTD.
Product details
Intended Use
Limited to the first level identification range of manual ophthalmic surgical instruments (M4350) of the Measures for the Administration of Medical Equipment.
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.4350 手動式眼科手術器械
Import Information
import
Dates and status
Registration Date
May 21, 2013
Expiry Date
May 21, 2023
About this record

Access comprehensive regulatory information for "Enmedia" Manual Eye Surgery Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 25faa38c5fb275ccffe17883a1427a86 and manufactured by AMIDIA LTD.. The authorized representative in Taiwan is VISIONRISE ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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+ Devices