Taiwan FDA registration 576f0c00f8b6c9a22d116b6ea1af9bb0
EPS EASYMAX Lanzo Lancing Device (Non-Sterile)
TW: 福永宜瑪氏雷碩採血筆(未滅菌)
Registration details
- Analysis ID
- 576f0c00f8b6c9a22d116b6ea1af9bb0
- License Form
- Ministry of Health Medical Device Import No. 021094
- Customs Code
- DHA09402109402
Company information
- Manufacturer
- GMMC (Global Medical Market Corporation)
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- EPS BIO TECHNOLOGY CORP.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 12, 2019
- Expiry Date
- Dec 12, 2024
About this record
Access comprehensive regulatory information for EPS EASYMAX Lanzo Lancing Device (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 576f0c00f8b6c9a22d116b6ea1af9bb0 and manufactured by GMMC (Global Medical Market Corporation). The authorized representative in Taiwan is EPS BIO TECHNOLOGY CORP..
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