What certifications does the product have?

The product is certified with CE and ISO13485.

How is the product packed?

One machine is packed in a black leather bag and a color box, with 50 boxes in one export carton.

What is the lead time for orders?

Peak season lead time is 1-3 months, while off-season lead time is one month.

High Quality Homecare Hospital Dual Head Stethoscope

Name: High Quality Homecare Hospital Dual Head Stethoscope
Brand: Ningbo Greetmed Medical Instruments Co., Ltd.
SKU: 846811845

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

Classification

Biological Diagnostics

Type

Blood Pressure Meter

Model NO.

PM010110005

Certification

CE, ISO13485

Group

Middle-aged and Old

Transport Package

Export Carton

Specification

CE, ISO, FDA

Trademark

Greetmed

Origin

China Zhejiang

Production Capacity

100000 Piece/Month

Key features

Dual Head Stethoscope: High quality homecare hospital dual head stethoscope included.

CE and ISO13485 Certified: Product holds CE and ISO13485 certifications for safety.

55mm Diameter Dial: Features a 55mm diameter dial for clear reading.

Plastic Shell Construction: Durable plastic shell design for lightweight use.

Excellent Stability: Provides stable measurements with anti-shake function.

6 Months Validity Period: Checkout period lasts 6 months with proper usage.

Versatile Application: Suitable for hospitals, clinics, ambulances, and home use.

Complete Component Set: Includes latex bulb, bladder, and nylon cuff.

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 validity period of the device?

If used properly and exactly, the checkout period lasts for 6 months.

Q: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%.

Q:What is the dial size?

The device features a 55mm diameter dial.

Q:What materials are used for the components?

The device includes a plastic shell, latex bulb, latex bladder, and nylon cuff.

Q:Where can this device be used?

It is suited for hospitals, clinics, ambulances, family use, and field rescue matters.