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Theoffie/Outudea-Ofie Human Placental Growth Factor Test Kit - Taiwan Registration ede1a02d07dd0198a5aa73fb724ed0dd

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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ede1a02d07dd0198a5aa73fb724ed0dd
Registration Details
Taiwan FDA Registration: ede1a02d07dd0198a5aa73fb724ed0dd
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Device Details

Theoffie/Outudea-Ofie Human Placental Growth Factor Test Kit
TW: ๅฒฑๅฅง่ฒ/ๆญๅœ–ๅฒฑๅฅง่ฒไบบ้กž่ƒŽ็›ค็”Ÿ้•ทๅ› ๅญๆชข้ฉ—ๅฅ—็ต„
Risk Class 2

Registration Details

ede1a02d07dd0198a5aa73fb724ed0dd

DHA05602707008

Company Information

Finland

Product Details

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

A Clinical chemistry and clinical toxicology

A.1585 Human placental prolactin testing system

import

Dates and Status

Feb 10, 2015

Feb 10, 2030