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tPSA Rapid Quantitative Test
Biotime
ProductNewReviewed

tPSA Rapid Quantitative Test

The tPSA Rapid Quantitative Test by Biotime is a fluorescent immunoassay designed for the quantitative determination of total Prostate-Specific Antigen (tPSA) in human serum. It provides a fast, precise, and reliable

Minimum Order1 Carton
Warranty1 Year
Regulatory ApprovalsWHO Prequalified, CFDA/NMPA, CE Marked, ISO 13485 Certified, FDA Approved
Country of OriginFlag of ChinaChina
BrandBiotime

Product Rating

This product has not been rated yet.

Description

The Biotime tPSA Rapid Quantitative Test measures total Prostate-Specific Antigen (tPSA) in human serum samples using a fluorescence immunoassay technique. PSA is a protein secreted by both normal and malignant prostate cells, and its concentration in blood is an essential indicator for assessing prostate cancer, benign prostatic hyperplasia (BPH), and prostatitis.

This rapid test offers clinicians a dependable method for early detection, risk assessment, and treatment monitoring of prostate-related conditions. The combination of speed, accuracy, and simplicity makes it suitable for use in urology departments, oncology centers, and clinical laboratories.

Key Features

  • Quantitative detection of total PSA in human serum
  • Rapid testing with results in just 15 minutes
  • High sensitivity and accuracy for prostate disease evaluation
  • Supports differential diagnosis of prostate disorders
  • Compatible with Biotime fluorescence analyzers
  • Convenient low-volume sampling for clinical use

Technical Specifications

Not specified.

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Standard Accessories

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Optional Accessories

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Package Contents

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Related Searches

TPSA Test Total Prostate Specific Antigen Test Prostate Health Screening Tumor Marker Test Fluorescence Immunoassay Quantitative Rapid Test POCT Diagnostic Kit
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Xiamen Biotime Biotechnology Co., Ltd Logo

Xiamen Biotime Biotechnology Co., Ltd

China FlagNo. 1565 Xiang’an North Road, Xiamen, Fujian, China

Reviewed manufacturer

Member Since

18 Oct 2025

Last Active

04 Aug 2026

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