Taiwan FDA registration 02d3575e390db1ad1496fa9dfafe3656
E-Kang heme test strip
TW: 易康 血紅素試紙
Taiwan·Risk Class 2·BIOPTIK TECHNOLOGY, INC.·Registered Apr 03, 2013 – Mar 22, 2026ExpiredRegistration details
- Analysis ID
- 02d3575e390db1ad1496fa9dfafe3656
Company information
- Manufacturer
- BIOPTIK TECHNOLOGY, INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- EASY LIFE GREEN TECHNOLOGY CORPORATION
Product details
- Intended Use
- Ekang heme test strip is an in vitro test reagent that can be used to self-measure the heme content of fingertip microvascular whole blood, but it is not suitable for newborn testing.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.7500 Whole blood hemoglobin analysis
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Apr 03, 2013
- Expiry Date
- Mar 22, 2026
About this record
Access comprehensive regulatory information for E-Kang heme test strip in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 02d3575e390db1ad1496fa9dfafe3656 and manufactured by BIOPTIK TECHNOLOGY, INC.. The authorized representative in Taiwan is EASY LIFE GREEN TECHNOLOGY CORPORATION.
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