Taiwan FDA registration 4e1a1966e7ab8bc9441bb013161898e3
“Eiken” PG Control
TW: “榮研” 胃蛋白酶原定量檢測試劑品管組
Registration details
- Analysis ID
- 4e1a1966e7ab8bc9441bb013161898e3
- License Form
- Ministry of Health Medical Device Import No. 027348
- Customs Code
- DHA05602734801
Company information
- Manufacturer
- EIKEN CHEMICAL CO., LTD NASU PLANT
- Manufacturer Country
- Japan
- Authorized Representative
- HUI SHENG INTERNATIONAL CORP.
Product details
- Intended Use
- This product is a low-concentration and high-concentration quality control substance, which is used in the determination of pepsinogen I and pepsinogen II in serum and plasma with reagents using automatic analysis equipment.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1660 Quality Control Materials (Analytical and Non-Analytical)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 10, 2015
- Expiry Date
- Jun 10, 2025
About this record
Access comprehensive regulatory information for “Eiken” PG Control in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4e1a1966e7ab8bc9441bb013161898e3 and manufactured by EIKEN CHEMICAL CO., LTD NASU PLANT. The authorized representative in Taiwan is HUI SHENG INTERNATIONAL CORP..
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