Taiwan FDA registration 50325a239f1336c781e5379c6bccf39e

Medtronic Manual Eye Surgery Instruments (Unsterilized)

TW: “美敦力”手動式眼科手術器械(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MEDTRONIC XOMED INSTRUMENTATION SAS·Registered Mar 26, 2010 – Mar 26, 2015Cancelled
Registration details
Analysis ID
50325a239f1336c781e5379c6bccf39e
Customs Code
DHA04400864807
Company information
Manufacturer Country
France
Authorized Representative
MEDTRONIC (TAIWAN) LTD.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Eye Surgery Instruments (M.4350)".
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
Mar 26, 2010
Expiry Date
Mar 26, 2015
Cancellation Date
Apr 25, 2018
Cancellation information
Status
Logged out
Reason
自行鍵入
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About this record

Access comprehensive regulatory information for Medtronic 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 50325a239f1336c781e5379c6bccf39e and manufactured by MEDTRONIC XOMED INSTRUMENTATION SAS. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MEDTRONIC XOMED, INC., 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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