"MOOHAN" Manual Surgical Instrument for General Use (Non-Sterile) - Taiwan Registration cb1d28d36851901281dcbb0eb448b471
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 cb1d28d36851901281dcbb0eb448b471 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
cb1d28d36851901281dcbb0eb448b471
Ministry of Health Medical Device Import No. 014406
DHA09401440601
Product Details
I General and plastic surgical devices
I4800 General Surgery Manual Instrument
Imported from abroad
Dates and Status
Aug 04, 2014
Aug 04, 2019
Aug 05, 2022
Cancellation Information
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"Moohan" Manual Surgical Instrument for General use (Non-Sterile)
MOOHAN ENTERPRISE CO., LTD
217d66306f1a2aa6c779d931e485045d
1
"MOOHAN" Manual Surgical Instrument for General Use (Non-Sterile)
MOOHAN ENTERPRISE CO., LTD
82f4d05ae9ac07d49bcdcbe2175e2eb5
1

