"Moohan" Manual Surgical Instrument for General use (Non-Sterile) - Taiwan Registration 217d66306f1a2aa6c779d931e485045d
Access comprehensive regulatory information for "Moohan" 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 217d66306f1a2aa6c779d931e485045d and manufactured by MOOHAN ENTERPRISE CO., LTD. The authorized representative in Taiwan is MEDI-CORE BIOTECH CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MOOHAN ENTERPRISE CO., LTD, and 2 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
217d66306f1a2aa6c779d931e485045d
Ministry of Health Medical Device Import No. 017687
DHA09401768701
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
Apr 07, 2017
Apr 07, 2022
"MOOHAN" Manual Surgical Instrument for General Use (Non-Sterile)
MOOHAN ENTERPRISE CO., LTD
82f4d05ae9ac07d49bcdcbe2175e2eb5
1
"MOOHAN" Manual Surgical Instrument for General Use (Non-Sterile)
MOOHAN ENTERPRISE CO., LTD
cb1d28d36851901281dcbb0eb448b471
1

