Taiwan FDA registration 5017f88904484d4cd4854e66705d3be2
“GMMC medisana” Lancing Device(Non-Sterile)
TW: 吉美美碩採血筆(未滅菌)
Registration details
- Analysis ID
- 5017f88904484d4cd4854e66705d3be2
- License Form
- Ministry of Health Medical Device Import No. 021588
- Customs Code
- DHA09402158801
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
- May 28, 2020
- Expiry Date
- May 28, 2025
About this record
Access comprehensive regulatory information for “GMMC medisana” 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 5017f88904484d4cd4854e66705d3be2 and manufactured by GMMC (Global Medical Market Corporation). The authorized representative in Taiwan is EPS BIO TECHNOLOGY CORP..
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices