Testsealabs PSA Prostate Specific Antigen Test Kit

Name: Testsealabs PSA Prostate Specific Antigen Test Kit
Brand: HangZhou Testsea biotechnology Co., Ltd.
SKU: 2265335885

Zhejiang, ChinaHangZhou Testsea biotechnology Co., Ltd.

US$0.50

1,000 Pieces

Sample price:US$0.10/piece.Request sample

Product profile

Customization

Available

Type

IVD Reagent

Certificate

ISO9001, ISO13485, CE

OEM/ODM

Support

Shelf life

2 Years

Samples

Support

Transport Package

Carton

Specification

25tests/box

Trademark

TESTSEALABS

Origin

China

HS Code

3822190090

Production Capacity

100000000

Key features

Rapid 15-Minute Results: Enables fast clinical decisions with results readable within 15 minutes.

High Sensitivity and Specificity: Provides accurate qualitative detection with high clinical reliability for prostate health screening.

Multi-Specimen Compatibility: Accepts whole blood, serum, or plasma on the same cassette for simplified workflow.

Small Sample Volume Required: Needs only 1 drop of serum/plasma or 2 drops of whole blood, reducing collection burden.

Built-in Procedural Control: Control line confirms proper specimen volume and membrane migration for valid results.

Simple Operation: No extra equipment needed; ideal for point-of-care and decentralized settings.

OEM/ODM Support Available: Custom packaging, branding, and inserts available for tailored solutions.

Comprehensive Certifications: ISO9001, ISO13485, and CE certified for quality and safety assurance.

Company profile

HangZhou Testsea biotechnology Co., Ltd.

Zhejiang, China

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service AvailableExport Year: 2022-04-08Nearest Port: Shanghai, Ningbo, ShenzhenAverage Response Time: ≤10.15h CertifiedTerms of Payment: LC, T/T, D/P

AI-Powered supplier vetting

SummaryTestsea Biotechnology is identified as a China-based limited company in Hangzhou, with records describing it as both a trading company and manufacturer/factory. Its stated capabilities include in-vitro diagnostic, veterinary, rapid-test, reagent, and medical-machine products. The supplier reports ISO 9001 and GMP certification, more than 10 production lines, 50 R&D engineers, 50 quality-control staff, and exports to multiple global regions. It describes three technical platforms and sales coverage exceeding 100 countries and regions. However, the evidence does not establish after-sales performance, financial credibility, or product-customization capability. One record associates the supplier with a 2025 THC urine-test product and a Vietnamese buyer, but this is limited customer evidence and does not independently verify broader performance.

Supplier typeThe supplier is identified as a limited company headquartered in Hangzhou, China, and is described as both a trading company/manufacturer-factory. A separate record characterizes the company nature as a factory, supporting a manufacturing role alongside trading activity.

CertificationsThe supplier reports ISO 9001 and GMP certification under its management-system certifications. These are explicit certifications relevant to quality and manufacturing controls.

R&D capabilityThe supplier states that it develops core innovative raw-material technologies and has established immunological detection, molecular-biology detection, and protein core-sheet inspection platforms. The reported 50 R&D engineers and continuing R&D investment further support an established innovation function.

Production capacityThe supplier reports more than 10 production lines, 50 quality-control staff, a one-month off-peak lead time, and broad diagnostic-product offerings. It also reports 90% export sales and access to Shanghai, Ningbo, and Shenzhen ports, although the stated peak-season fulfillment time of 6–12 months indicates substantial seasonal capacity constraints.

Client casesThe supplier states that its products have been sold in more than 100 countries and regions. A separate record identifies a THC urine-test product and one associated Vietnamese buyer, but it does not provide verifiable case details such as order scale, duration, performance results, or references.

Product Q&A

Q:What is this product used to detect?

This product is a rapid qualitative immunochromatographic assay for the detection of prostate specific antigen (PSA) in human whole blood, serum or plasma. It is intended as a screening aid for prostate health and clinical reference.

Q:What specimen volumes are required?

Serum or plasma: only 1 drop (approximately 30 microliters) plus 1 drop of buffer. Whole blood: 2 drops (approximately 60 microliters) plus 1 drop of buffer.

Q:How long does the test take and when should results be read?

Read the result at 15 minutes after adding specimens. Do not interpret after 20 minutes, as non-specific reactions may occur.

Q:How should the kit be stored?

Store in the sealed foil pouch at room temperature (4-30 degrees Celsius). Do not freeze. Stable through the expiration date printed on the pouch. Open the pouch only just before use.

Q:What are the typical application scenarios for this product?

Ideal for urology clinics, health check-up centers, community screening, emergency departments and primary care facilities as a rapid initial screening tool for at-risk populations, especially in settings without large automated analyzers.