What are the storage requirements?

Store indoors at temperatures between -5 and +35 degrees Celsius, with no corrosive gas, excellent ventilation, and relative humidity not exceeding 80%.

How can cross-infection be avoided?

It is recommended that the chest piece should be disinfected regularly to avoid cross-infection.

What certifications does this product have?

The product is certified with CE and ISO13485 standards.

Medical Pediatric Single Head Stethoscope

Name: Medical Pediatric Single Head Stethoscope
Brand: Ningbo Greetmed Medical Instruments Co., Ltd.
SKU: 674822645

Zhejiang, ChinaNingbo Greetmed Medical Instruments Co., Ltd.

US$1.00-10.00

5,000 Pieces

Product profile

Customization

Available

Classification

Biological Diagnostics

Type

Stethoscope

Model NO.

Gt002-120

Certification

CE, ISO13485

Transport Package

Export Carton

Specification

CE, ISO13485, FDA

Trademark

Greetmed

Origin

China Zhejiang

Production Capacity

100000 Piece/Month

Key features

Professional Pediatric Design: Specially designed for neonatal babies and children to diagnose heart and organ disorders.

High-Quality Materials: Features a silver chest piece, Y-type tubing, and plastic earpieces for durability and sound transmission.

CE and ISO13485 Certified: Meets international safety and quality standards with CE and ISO13485 certifications.

Non-Invasive and Safe: A conventional, non-active medical device with very low risk for patient safety.

12-Month Validity Period: Ensures reliable performance with a 12-month validity period when used properly.

Flexible Earpiece Design: Features a 'U' shaped band that can be manually adjusted for comfortable wear.

Company profile

Ningbo Greetmed Medical Instruments Co., Ltd.

Zhejiang, China

Business Type: Manufacturer/Factory, Trading CompanyExport Year: 2003-06-06Nearest Port: shanghaiAverage Response Time: ≤15hTerms 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 is the intended use of this stethoscope?

It is professionally designed for neonatal babies and children to diagnose disorders or diseases associated with the heart, arteries, and other internal organs.

Q:What materials are used in the stethoscope?

The stethoscope features a silver chest piece, Y-type tubing for sound transmission, a binaural tube, and plastic earpieces.

Q:How should the stethoscope be used?

Connect the earpiece and head with the latex tube, touch the patient with the membrane side, place earpieces comfortably in ears, and listen carefully. Adjust the 'U' shaped band for comfort.

Q:Is this device safe for children?

Yes, it is a conventional medical device with very low risk. It is non-invasive and non-active, making it safe for pediatric use.

Q:What is the validity period of the product?

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