"EMI" Manual Surgical Instrument for General Use (Non-sterile) - Taiwan Registration f959cfcd1a2f8bca6020d78a77dddcbd
Access comprehensive regulatory information for "EMI" 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 f959cfcd1a2f8bca6020d78a77dddcbd and manufactured by EMI FACTORY CO., LTD.. The authorized representative in Taiwan is GEMMGTAI CO..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including EMI FACTORY CO., LTD., 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.
Device Details
Registration Details
f959cfcd1a2f8bca6020d78a77dddcbd
Ministry of Health Medical Device Import No. 019332
DHA09401933200
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 19, 2018
Jul 19, 2023

