Taiwan FDA registration d3092e846ad84b486cbd014e89a5af67
"Fertipro" SpermMar (Non-Sterile)
TW: "費提普羅" 精蟲免疫抗體檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·MD·FERTIPRO N.V.·Registered Mar 30, 2016 – Mar 30, 2026ExpiredRegistration details
- Analysis ID
- d3092e846ad84b486cbd014e89a5af67
- License Form
- Ministry of Health Medical Device Import No. 016336
- Customs Code
- DHA09401633603
Company information
- Manufacturer
- FERTIPRO N.V.
- Manufacturer Country
- Belgium
- Authorized Representative
- ESSENCE EQUIP CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Human Whole Plasma or Serum Immunoassay System (C.5700)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C5700 Human whole plasma or serum immunoassay system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 30, 2016
- Expiry Date
- Mar 30, 2026
About this record
Access comprehensive regulatory information for "Fertipro" SpermMar (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 d3092e846ad84b486cbd014e89a5af67 and manufactured by FERTIPRO N.V.. The authorized representative in Taiwan is ESSENCE EQUIP CO., LTD..
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