"MOOHAN" Manual Surgical Instrument for General Use (Non-Sterile)
Taiwan·Risk Class 1·MD·MOOHAN ENTERPRISE CO., LTD·Registered Feb 18, 2016 – Feb 18, 2021Cancelled- Analysis ID
- 82f4d05ae9ac07d49bcdcbe2175e2eb5
- License Form
- Ministry of Health Medical Device Import No. 016173
- Customs Code
- DHA09401617301
- Manufacturer
- MOOHAN ENTERPRISE CO., LTD
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Taiwan Shenhe Co., Ltd
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
- Registration Date
- Feb 18, 2016
- Expiry Date
- Feb 18, 2021
- Cancellation Date
- Aug 22, 2017
- Status
- Logged out
- Reason
- 公司歇業
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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.