Pure Global

“Ditron” Manual Surgical Instrument for General Use (Non-Sterile) - Taiwan Registration 704c2b2e963c26a27bbdf5deee929068

Access comprehensive regulatory information for “Ditron” 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 704c2b2e963c26a27bbdf5deee929068 and manufactured by DITRON DENTAL LTD.. The authorized representative in Taiwan is TUNG SHENG MEDICAL INC..

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
704c2b2e963c26a27bbdf5deee929068
Registration Details
Taiwan FDA Registration: 704c2b2e963c26a27bbdf5deee929068
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

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

Registration Details

704c2b2e963c26a27bbdf5deee929068

Ministry of Health Medical Device Import No. 021700

DHA09402170005

Company Information

Israel

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

Jul 03, 2020

Jul 03, 2025