"MOOHAN" Manual Surgical Instrument for General Use (Non-Sterile)
Taiwan·Risk Class 1·MD·MOOHAN ENTERPRISE CO., LTD·Registered Aug 04, 2014 – Aug 04, 2019Cancelled- Analysis ID
- cb1d28d36851901281dcbb0eb448b471
- License Form
- Ministry of Health Medical Device Import No. 014406
- Customs Code
- DHA09401440601
- Manufacturer
- MOOHAN ENTERPRISE CO., LTD
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- MEDI-CORE BIOTECH 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
- Aug 04, 2014
- Expiry Date
- Aug 04, 2019
- Cancellation Date
- Aug 05, 2022
- Status
- Logged out
- Reason
- 未展延而逾期者
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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 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.