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"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.

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cb1d28d36851901281dcbb0eb448b471
Registration Details
Taiwan FDA Registration: cb1d28d36851901281dcbb0eb448b471
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Device Details

"MOOHAN" Manual Surgical Instrument for General Use (Non-Sterile)
TW: "้ป˜็ฝ•"ไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

cb1d28d36851901281dcbb0eb448b471

Ministry of Health Medical Device Import No. 014406

DHA09401440601

Company Information

Korea, Republic of

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

Logged out

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