Taiwan FDA registration 4e25efc20ad64b1f5d6aa363ac516937
“MEDICORE” Heart Rate Variability Analysis Equipment
TW: “麥迪科”心律變異分析器
Taiwan·Risk Class 2·MD·MEDICORE CO., LTD.·Registered Jul 31, 2018 – Jul 31, 2028ActiveRegistration details
- Analysis ID
- 4e25efc20ad64b1f5d6aa363ac516937
- License Form
- Ministry of Health Medical Device Import No. 031230
- Customs Code
- DHA05603123006
Company information
- Manufacturer
- MEDICORE CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- NEWAED WORLDWIDE PROCUREMENT CONGLOMERATE CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E2780 Hydraulic, pneumatic or photoelectric plethysmron
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 31, 2018
- Expiry Date
- Jul 31, 2028
About this record
Access comprehensive regulatory information for “MEDICORE” Heart Rate Variability Analysis Equipment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4e25efc20ad64b1f5d6aa363ac516937 and manufactured by MEDICORE CO., LTD.. The authorized representative in Taiwan is NEWAED WORLDWIDE PROCUREMENT CONGLOMERATE CORPORATION.
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