What is the lead time for orders?

The lead time is 1-3 months during peak season and one month during the off-season.

What payment terms are accepted?

We accept LC (Letter of Credit) and T/T (Telegraphic Transfer) as terms of payment.

Antigen Rapid Test Self-Testing Medical Pockets Diagnostic Test Kits

Name: Antigen Rapid Test Self-Testing Medical Pockets Diagnostic Test Kits
Brand: Ningbo Greetmed Medical Instruments Co., Ltd.
SKU: 1956007765

Zhejiang, ChinaNingbo Greetmed Medical Instruments Co., Ltd.

US$0.90-0.95

100,000 Pieces

Sample price:US$10.00/piece.Request sample

Product profile

Customization

Available

Type

IVD Reagent

Item

Antigen Rapid Test

Model NO.

GT-TK-010

After-Sale Service

Online Technical Support

Transport Package

Box

Specification

Antigen Rapid Test

Trademark

Greetmed

Origin

China

Production Capacity

500000 Pieces Per Day

Key features

Self-Testing Convenience: Authorized for prescription home use with anterior nasal swab samples for patient self-testing.

High Accuracy Comparison: Test cassettes compared with commercial PCR, ensuring reliable diagnostic results.

Comprehensive Kit Contents: Includes 5 test cassettes, extraction kits, sterile swabs, tube holder, and biohazard waste bags.

Global Certifications: Certified by CE0123, ISO13485:2003, and FDA for quality and safety standards.

OEM/ODM/OBM Support: Leading manufacturer offering customized branding and manufacturing services for global clients.

Online Technical Support: Provides dedicated online technical support services for after-sale assistance.

Wide Market Reach: Products sold to North America, Europe, Asia, Africa, and other international markets.

Company profile

Ningbo Greetmed Medical Instruments Co., Ltd.

Zhejiang, China

Business Type: Manufacturer/Factory, Trading CompanyExport Year: 2003-06-06Nearest Port: shanghaiAverage Response Time: ≤18hTerms of Payment: LC, T/TInternational Commercial Terms(Incoterms): FOB, CIF

AI-Powered supplier vetting

SummaryGREETMED demonstrates OEM and ODM capability, broad customization options, recent new-product activity, and stated quality-control procedures with material traceability. It reports ERP-based process digitization, CE certification capability, participation in MEDICA 2025, and procedures for corrective actions and complaint handling. However, it has no overseas showroom, agent, or branch, reports zero countries with overseas services, lacks an SDK, and has no fixed-source pollution registration or factory environmental impact assessment report. Supplier-assessment procedures are documented but lack records, and the stated peak-season lead-time information is inconsistent, limiting confidence in operational evaluation.

Supplier typeThe supplier is identified through the GREETMED own-brand reference and reports both OEM services for well-known brands and ODM services. Its offerings therefore support classification as a manufacturer with own-brand, OEM, and ODM capabilities, although the slices do not provide a formal legal or industry classification.

CertificationsThe supplier reports CE certification capability, which is explicit evidence of holding or supporting this product certification. No broader certification portfolio is provided, so the assessment is limited to CE.

After-Sales capabilityThe supplier has documented corrective and preventive action and customer-complaint procedures with follow-up records, and describes professional after-sales support. However, it has no overseas showroom, agent, or branch and reports zero countries with overseas services; service assessment procedures exist without records, indicating strong stated internal handling but limited overseas coverage and verification.

R&D capabilityThe supplier reports new products during the past year, ODM capability, and enterprise digitalization through ERP, with additional digital-development indicators recorded. It does not have an available SDK, but that limitation does not negate the demonstrated product-development and process-digitization evidence.

Production capacityProduction capability is supported by stated advanced equipment, standardized operations, quality-assurance processes, material traceability, written work instructions, and uniformly followed inspections. The supplier also reports 30 qualified suppliers, but its service-capability assessment procedure has no records and the peak-season lead-time entry is internally inconsistent, so operational verification remains incomplete.

Customization capabilityThe supplier explicitly offers customization from samples and designs, full and minor customization, flexible customization, and ODM services. This is direct evidence of broad customization capability.

Client casesThe supplier reports OEM service for well-known brands and participation in the offline MEDICA 2025 trade show. These are evidence of brand-serving experience and market exposure, but no named customer cases or project details are provided.

Product Q&A

Q:What type of sample is required for this test?

The test requires anterior nasal (nares) swab samples for collection.

Q:Can this test be used at home?

Yes, this test is authorized for prescription home use and can be performed by patients themselves.

Q:What certifications does the product have?

The product is certified by CE0123, ISO13485:2003, and FDA.

Q:Is OEM or ODM service available?

Yes, we supply clients with OEM, ODM, or OBM services for customized products.

Q:What items are included in the package?

The package includes 5 test cassettes, 5 extraction kits, 5 sterile swabs, 1 package insert, 1 tube holder, 5 biohazard waste bags, and 1 qualification certificate.

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Antigen Rapid Test Self-Testing Medical Pockets Diagnostic Test Kits