Taiwan FDA registration d19a99c45a70c4be02fb81ffce2879f8
GB S-TSH (U-TSH) EIA Kit
TW: 普生超靈敏甲狀腺刺激素酵素免疫分析套組
Registration details
- Analysis ID
- d19a99c45a70c4be02fb81ffce2879f8
- License Form
- Ministry of Health Medical Device Import No. 026817
- Customs Code
- DHA05602681705
Company information
- Manufacturer
- BioCheck, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- GENERAL BIOLOGICALS CORP.
Product details
- Intended Use
- Quantitatively measure the concentration of thyroid-stimulating hormone (TSH) in human serum.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1690 Thyroid Stimulation Hormone Test System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 18, 2014
- Expiry Date
- Dec 18, 2024
About this record
Access comprehensive regulatory information for GB S-TSH (U-TSH) 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 d19a99c45a70c4be02fb81ffce2879f8 and manufactured by BioCheck, Inc.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices