"Molnlycke" Manual surgical instrument for general use (Non-Sterile)
Taiwan·Risk Class 1·MD·MOLNLYCKE HEALTH CARE AB·Registered Jun 26, 2015 – Jun 26, 2020Cancelled- Analysis ID
- 956c7144aee59bdc5b25a364afd6f724
- License Form
- Ministry of Health Medical Device Import No. 015385
- Customs Code
- DHA09401538501
- Manufacturer
- MOLNLYCKE HEALTH CARE AB
- Manufacturer Country
- United States
- Authorized Representative
- LYRA 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
- Jun 26, 2015
- Expiry Date
- Jun 26, 2020
- Cancellation Date
- Jul 15, 2022
- Status
- Logged out
- Reason
- 未展延而逾期者
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Access comprehensive regulatory information for "Molnlycke" 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 956c7144aee59bdc5b25a364afd6f724 and manufactured by MOLNLYCKE HEALTH CARE AB. The authorized representative in Taiwan is LYRA LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MOLNLYCKE HEALTH CARE AB, and 1 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.