Taiwan FDA registration e1faba1697380bd3da46044de911335d
"Yifu" dry heme determination system
TW: “醫福”乾式血紅素測定系統
Registration details
- Analysis ID
- e1faba1697380bd3da46044de911335d
- Customs Code
- DHA05603355100
Company information
- Manufacturer
- EKF-diagnostic GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- AMESDATA BIOTECH CO., LTD.
Product details
- Intended Use
- This product is used to quantitatively determine the concentration of hemoglobin (Hb) in human blood.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.7500 Whole blood hemoglobin analysis
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Sep 03, 2020
- Expiry Date
- Sep 03, 2025
About this record
Access comprehensive regulatory information for "Yifu" dry heme determination system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e1faba1697380bd3da46044de911335d and manufactured by EKF-diagnostic GmbH. The authorized representative in Taiwan is AMESDATA BIOTECH CO., LTD..
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