Taiwan FDA registration 32cfcc81600208aedb03180a334b076f

"Junfeng" manual ophthalmic surgery instrument (unsterilized)

TW: "鈞豊"手動式眼科手術器械(未滅菌)
Taiwan flagTaiwan·Risk Class 1·Suqian Zhengtong Medical Instruments Co., Ltd.;; Jiangsu Konska Medical Instrument Ltd.·Registered Feb 12, 2015 – Feb 12, 2030Active
Registration details
Analysis ID
32cfcc81600208aedb03180a334b076f
Customs Code
DHA09600233402
Company information
Manufacturer Country
China
Authorized Representative
JUN FENG OPTICAL CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of the "Manual Ophthalmic Surgical Instruments (M.4350)" of the Measures for the Classification and Grading 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
QMS/QSD;; 委託製造
Dates and status
Registration Date
Feb 12, 2015
Expiry Date
Feb 12, 2030
About this record

Access comprehensive regulatory information for "Junfeng" manual ophthalmic surgery instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 32cfcc81600208aedb03180a334b076f and manufactured by Suqian Zhengtong Medical Instruments Co., Ltd.;; Jiangsu Konska Medical Instrument Ltd.. The authorized representative in Taiwan is JUN FENG OPTICAL 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