David Ce/FDA Approved 2.8mm HCG Cassette Test Kit

Name: David Ce/FDA Approved 2.8mm HCG Cassette Test Kit
Brand: Equinox Biotech Co., Ltd.
SKU: 780149392

Guangdong, ChinaEquinox Biotech Co., Ltd.

US$0.12-0.30

5,000 Pieces

Product profile

Type

IVD Instrument

Sensitivity

10 Miu/Ml;15miu/Ml;25miu/Ml

Accuracy

More Than 99%

Model NO.

RH-HCG-C

Shelf Time

24-36 Month

Specimen

Urine, Serum

Certificate

Ce/ISO13485/FDA

Format

Strip /Cassette /Midstream

Transport Package

Individual Packed in Foil Pouch

Specification

2.8mm/3.0mm/4.0. mm

Trademark

DAVID, RUNBIO, OEM

Origin

Shantou, China

Production Capacity

400000 Piece/Pieces Per Day

Company profile

Equinox Biotech Co., Ltd.Guangdong, China

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Customization from Samples, Customization from Designs, etc. CertifiedExport Year: 20 years CertifiedNearest Port: Shantou Port, Shenzhen PortAverage Response Time: ≤18h

AI-Powered supplier vetting

SummaryThe supplier is a combined company engaged in cosmetics, sanitary products, disposable medical supplies, personal hygiene products, and related sales activities. It demonstrates broad customization, ODM, OEM, 3D design, and R&D capabilities, supported by documented design inputs, outputs, reviews, verification, and confirmation. Quality and service procedures are documented and followed, including complaint handling, corrective and preventive actions, and finished-product inspection. Manufacturing support includes valid contracts with associated subcontractors and in-stock capability, while lead times are within 15 working days off-season and one month during peak season. Overseas service infrastructure is limited: there are no overseas warehouses, showrooms, agents, or branches, and overseas service countries are listed as zero. Financial credibility and formal certifications cannot be sufficiently assessed from the provided information.

Supplier typeThe supplier is identified as a combined company. Its stated business scope covers production and sales of cosmetics, sanitary products, disposable medical supplies, and personal hygiene products, subject to any legally required approvals.

After-Sales capabilityThe supplier has documented and followed procedures for customer complaints and corrective and preventive actions, and its technology engineers provide technical support for production and after-sales service. However, it has no overseas agents, branches, showrooms, or warehouses, which limits the documented overseas service infrastructure.

R&D capabilityThe supplier reports new products during the past year, provides ODM services, and maintains R&D audit documentation covering design inputs, outputs, reviews, verification, and confirmation. Its engineers are responsible for new product development and technical support, indicating documented and active innovation capability.

Production capacityProduction-related controls include quality assurance, uniformly followed finished-product inspection instructions, valid manufacturing-capacity contracts with associated subcontractors, and in-stock capability. Stated lead times are within 15 working days off-season and one month during peak season, supporting an established production and fulfillment capability.

Customization capabilityThe supplier offers customization from samples and designs, full, minor, and flexible customization, plus 3D software design services and ODM services. These explicit service offerings indicate broad customization capability, although no SDK is available.

Client casesThe supplier reports OEM service for well-known brands and participation in the HOSPITALAR 2023 offline trade show. These are evidence of market-service experience, but no specific customer names, product projects, outcomes, or independently verifiable case details are provided.