Taiwan FDA registration 1cdfc4b02cb86de005da5f3bd7ae6714
“Randox” Discrete photometric chemistry analyzer for clinical use (Non-Sterile)
TW: “瑞德士” 臨床使用的個別式光度量測化學分析儀 (未滅菌)
Registration details
- Analysis ID
- 1cdfc4b02cb86de005da5f3bd7ae6714
- License Form
- Ministry of Health Medical Device Import Registration No. a00011
- Customs Code
- DHA084a0001102
Company information
- Manufacturer
- RANDOX LABORATORIES LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- KUO'S YUAN IN ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Individual Photometric Chemistry Analyzer for Clinical Use (A.2160)" of the Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A2160 Individual photometric chemistry analyzer for clinical use
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 22, 2021
- Expiry Date
- Oct 31, 2023
About this record
Access comprehensive regulatory information for “Randox” Discrete photometric chemistry analyzer for clinical use (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1cdfc4b02cb86de005da5f3bd7ae6714 and manufactured by RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is KUO'S YUAN IN ENTERPRISE CO., LTD..
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