Taiwan FDA registration 246119fe50db192f5884b60643b48ddf
GB β2-Microglobulin EIA Kit
TW: 普生β2-微球蛋白酵素免疫分析套組
Taiwan·Risk Class 2·MD·BioCheck, Inc.·Registered Jun 26, 2015 – Jun 26, 2025ExpiredRegistration details
- Analysis ID
- 246119fe50db192f5884b60643b48ddf
- License Form
- Ministry of Health Medical Device Import No. 027361
- Customs Code
- DHA05602736106
Company information
- Manufacturer
- BioCheck, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- GENERAL BIOLOGICALS CORP.
Product details
- Intended Use
- Quantitatively detect the concentration of β2-microglobulin in human serum.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C5630 β-2-Microglobulin Immunoassay System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 26, 2015
- Expiry Date
- Jun 26, 2025
About this record
Access comprehensive regulatory information for GB β2-Microglobulin EIA Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 246119fe50db192f5884b60643b48ddf and manufactured by BioCheck, Inc.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
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