What is the test method used in this kit?

The kit uses the PCR-Fluorescent Probe Method for detection.

Foot-and-Mouth Disease Virus Universal (FMDV-U) Detection Kit Rt-PCR Kit

Name: Foot-and-Mouth Disease Virus Universal (FMDV-U) Detection Kit Rt-PCR Kit
Brand: Changsha Renji Medical Equipments Co., Ltd.
SKU: 1925717471

Hunan, ChinaChangsha Renji Medical Equipments Co., Ltd.

US$2.00

5,000-99,999 Pieces

US$1.50

100,000+ Pieces

Sample price:US$1.00/piece.Request sample

Product profile

Customization

Available

Classification

Biological Diagnostics

Type

Animal Disease Diagnostic Kit

Model NO.

ZB-R-011

Certification

CE, ISO13485

Group

Pig

Specificity

Foot-and-Mouth Disease Virus(Fmdv-U)

Species

Virus

Nucleic Acid Type

DNA

Sanples

Available

Test Method

PCR-Fluorescent Probe Method

OEM

Accepted

Storage

Store at -20degree

Specification

48T

Trademark

Renji

Origin

China

HS Code

9018390000

Production Capacity

1000000/Day

Key features

High Sensitivity Detection: Optimized dNTPs and PCR enhancers maximize sensitivity for FMDV-U detection.

High Specificity: Proprietary technology uses monoclonal antibodies to block Taq polymerase activity.

Minimal Cross-Contamination: Incorporates dUTP/UDG system to degrade Uracil-containing DNA and eliminate contamination.

Wide Sample Compatibility: Compatible with a wider range of sample types due to specific enzyme blocking technology.

High Throughput Capacity: Capable of detecting up to 48 individual samples or pooled samples simultaneously.

Broad Instrument Compatibility: Works with MA-6000, ABI, Bio-Rad, Roche, Cepheid, and Rotor-Gene series detectors.

OEM Service Available: Original Equipment Manufacturer service is accepted for customized orders.

CE and ISO13485 Certified: Product holds CE, ISO13485, and SGS certifications for quality assurance.

Company profile

Self-brandedStandardized quality controlR&D CapabilitiesManagement Certification

Changsha Renji Medical Equipments Co., Ltd.

Hunan, China

Business Type: Manufacturer/Factory, Trading CompanyExport Year: 2020-10-01Nearest Port: guangzhou, shenzhen, shanghaiAverage Response Time: ≤6.79hTerms of Payment: LC, T/T, D/P, etc.International Commercial Terms(Incoterms): FOB, CFR, CIF, FCA, EXW

AI-Powered supplier vetting

SummaryThe supplier is identified as a manufacturing factory producing sanitary materials, medical supplies, medical devices, disinfection products, and sanitary equipment. It reports customization from samples, designs, and full specifications, with two production lines and export markets spanning multiple regions. Quality and service procedures are documented, and the supplier states that it holds or has products approved by CE, SGS, ISO13485, NMPA, and ISO9001:2015-related certification. It also reports OEM service for known brands and experience exporting to more than 50 countries. However, no SDK is available, and the supplier lacks in-stock service, overseas warehouse, overseas showroom, and a valid manufacturing-capacity contract with affiliated subcontractors. Financial information is represented only by years rather than usable performance figures, so financial credibility cannot be determined.

Supplier typeThe supplier is explicitly identified as a factory, with a business scope covering manufacturing of sanitary materials, medical supplies, medical devices, disinfection products, and sanitary equipment. Its associated companies are classified in manufacturing, supporting a direct manufacturing-supplier profile.

CertificationsThe supplier reports an ISO9001:2015 certificate and states that its products have been approved by CE, SGS, ISO13485, and NMPA, among others. These stated certifications and approvals provide explicit evidence of certification coverage, although the slices do not provide certificate numbers, validity dates, or scope details.

After-Sales capabilityThe supplier reports written and followed procedures for service-capability assessment, corrective and preventive actions, and customer complaint handling. This is explicit evidence of a documented after-sales and complaint-management system.

R&D capabilityThe supplier explicitly reports no available SDK, which limits evidence of software-development or integration capability. Although it emphasizes product certifications and customer-oriented management, the slices do not establish broader research, product-development, or innovation performance.

Production capacityThe supplier operates two production lines, reports peak-season fulfillment of one month and off-peak lead time within 15 working days, and has export access through major Chinese ports. However, it reports no in-stock capacity and no valid manufacturing-capacity contract with affiliated subcontractors, creating explicit operational limitations despite its stated factory capacity.

Customization capabilityThe supplier explicitly offers customization from samples, designs, and full customization, and also reports OEM service for known brands. These capabilities directly support customized and OEM manufacturing requirements.

Client casesThe supplier states that it provides OEM services for known brands and has export experience involving more than 50 countries. These statements indicate brand-related and international customer experience, but no specific customer names, project details, or independently verifiable cases are provided.