Taiwan FDA registration ede1a02d07dd0198a5aa73fb724ed0dd
Theoffie/Outudea-Ofie Human Placental Growth Factor Test Kit
TW: 岱奧菲/歐圖岱奧菲人類胎盤生長因子檢驗套組
Taiwan·Risk Class 2·WALLAC OY·Registered Feb 10, 2015 – Feb 10, 2030ActiveRegistration details
- Analysis ID
- ede1a02d07dd0198a5aa73fb724ed0dd
- Customs Code
- DHA05602707008
Company information
- Manufacturer
- WALLAC OY
- Manufacturer Country
- Finland
- Authorized Representative
- FENG CHI BIOTECH CORP.
Product details
- Intended Use
- This test kit is used to quantify the concentration of human placental growth factor (PlGF) in maternal serum. Can use the Auto DELFIA automatic immunoassay system or the DELFIA system
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1585 Human placental prolactin testing system
- Import Information
- import
Dates and status
- Registration Date
- Feb 10, 2015
- Expiry Date
- Feb 10, 2030
About this record
Access comprehensive regulatory information for Theoffie/Outudea-Ofie Human Placental Growth Factor Test Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ede1a02d07dd0198a5aa73fb724ed0dd and manufactured by WALLAC OY. The authorized representative in Taiwan is FENG CHI BIOTECH CORP..
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