Pure Global

“Vycor” Manual Surgical Instrument for General Use (Non-Sterile) - Taiwan Registration ef562a8a4a1dde54e9cb77aaebb2fa8e

Access comprehensive regulatory information for “Vycor” Manual Surgical Instrument for General Use (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ef562a8a4a1dde54e9cb77aaebb2fa8e and manufactured by VYCOR MEDICAL INC.. The authorized representative in Taiwan is MATECH HEALTHCARE CORPORATION.

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 Database
Powered by Pure Global AI
89,000+ Devices
ef562a8a4a1dde54e9cb77aaebb2fa8e
Registration Details
Taiwan FDA Registration: ef562a8a4a1dde54e9cb77aaebb2fa8e
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Vycor” Manual Surgical Instrument for General Use (Non-Sterile)
TW: “博科”一般手術用手動式器械(未滅菌)
Risk Class 1
MD

Registration Details

ef562a8a4a1dde54e9cb77aaebb2fa8e

Ministry of Health Medical Device Import No. 013979

DHA09401397904

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".

I General and plastic surgical devices

I4800 General Surgery Manual Instrument

Imported from abroad

Dates and Status

Mar 21, 2014

Mar 21, 2024