How should the stethoscope be stored?

Store indoors at -5 to +35 degrees Celsius with humidity under 80% and no corrosive gas.

What is the validity period of the product?

If used properly, the checkout period lasts for 12 months.

High quality Deluxe Single Head Stethoscope

Name: High quality Deluxe Single Head Stethoscope
Brand: Ningbo Greetmed Medical Instruments Co., Ltd.
SKU: 674823065

Zhejiang, ChinaNingbo Greetmed Medical Instruments Co., Ltd.

US$1.00-10.00

1,000 Pieces

Sample price:US$5.00/piece.Request sample

Product profile

Customization

Available

Sterilization

Non Sterilization

Feature

Reusable

Model NO.

PM010110002

Application

Clinical, Household

Material

Metal

Certification

CE, ISO13485

Power Type

Without Power

Group

Adult

Transport Package

Export Carton: 570X480X270mm

Specification

CE\TUV

Trademark

Greetmed

Origin

China Zhejiang

Production Capacity

1000000 Piece/Month

Key features

CE, ISO13485 & FDA Certified: Certified by CE0123, ISO13485:2003 and FDA for quality assurance.

Durable Zinc Alloy Construction: Features a zinc alloy chest piece with chrome plated silver finish.

OEM/ODM/OBM Support: We supply clients with OEM, ODM, or OBM services to meet needs.

Competitive Pricing: Reasonable and competitive prices to help occupy your market.

Fast Response Time: We reply to emails or faxes within 18 hours of enquiry.

Professional Technical Support: Dedicated staff provide technical support and after-sales service.

Reusable Medical Device: Non-invasive, non-active device for diagnosing heart and lung sounds.

Standardized Quality Control: Advanced production technology and strict management ensure quality.

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.