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"MOOHAN" Manual Surgical Instrument for General Use (Non-Sterile) - Taiwan Registration 82f4d05ae9ac07d49bcdcbe2175e2eb5

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 82f4d05ae9ac07d49bcdcbe2175e2eb5 and manufactured by MOOHAN ENTERPRISE CO., LTD. The authorized representative in Taiwan is Taiwan Shenhe 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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82f4d05ae9ac07d49bcdcbe2175e2eb5
Registration Details
Taiwan FDA Registration: 82f4d05ae9ac07d49bcdcbe2175e2eb5
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Device Details

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

Registration Details

82f4d05ae9ac07d49bcdcbe2175e2eb5

Ministry of Health Medical Device Import No. 016173

DHA09401617301

Company Information

Korea, Republic of

Product Details

I General and plastic surgical devices

I4800 General Surgery Manual Instrument

Imported from abroad

Dates and Status

Feb 18, 2016

Feb 18, 2021

Aug 22, 2017

Cancellation Information

Logged out

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