Taiwan FDA registration 7d201f3564b42dae2a10b64167a58be9
MeDiPro Cystatin C Calibrator Set
TW: 台塑生醫胱蛋白C校正液組
Registration details
- Analysis ID
- 7d201f3564b42dae2a10b64167a58be9
- License Form
- Ministry of Health Medical Device Manufacturing No. 004948
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- FORMOSA BIOMEDICAL TECHNOLOGY CORPORATION
Product details
- Intended Use
- This product is used for the calibration of Formosa Biomedical Cystin C Reagent, and is used with Formosa Biomedical Cystin C Reagent and automatic biochemical analyzer Hitachi7170/917 machine.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1150 calibrate
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Aug 07, 2015
- Expiry Date
- Aug 07, 2025
About this record
Access comprehensive regulatory information for MeDiPro Cystatin C Calibrator Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7d201f3564b42dae2a10b64167a58be9 and manufactured by Formosa Biomedical Technology Co., Ltd. Yilan Factory. The authorized representative in Taiwan is FORMOSA BIOMEDICAL TECHNOLOGY CORPORATION.
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