Foreign Matter Removing Device Rescue Instrument with Updated Design

Name: Foreign Matter Removing Device Rescue Instrument with Updated Design
Brand: Ningbo Hanyue Medical Technology Co.,Ltd
SKU: 1966393151

Zhejiang, ChinaNingbo Hanyue Medical Technology Co.,Ltd

US$3.00-5.60

500 Sets

Sample price:US$10.00/set.Request sample

Product profile

Customization

Available

Material

PVC

Application

Travel, Hospital, Vehicle, Factory, Office, Homecare

Model NO.

HY-101

Type

Emergency Rescue Device

Size

3 Sizes in 1 Set

Certification

CE, FDA, ISO13485

Hardness

Medium

Style

Simple

Logo Printing

Without Logo Printing

Group

All

Feature

Disposable

Packing

Transparent Bag Packing

Mask Size

Pediatric, Adult M, Adult L

Transport Package

Carton

Specification

3 sizes fit for all people

Trademark

Hanwell

Origin

China

HS Code

9020000000

Production Capacity

500000/Month

Company profile

Importers and ExportersHigh Repeat Buyers ChoiceSelf-branded

Ningbo Hanyue Medical Technology Co.,Ltd

Zhejiang, China

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available CertifiedCustomization Options: Customization from Samples, Customization from Designs, etc. CertifiedExport Year: 3 Years CertifiedNearest Port: Ningbo Port, Shanghai PortAverage Response Time: ≤2.41h

AI-Powered supplier vetting

SummaryNingbo Hanyue Medical Technology Co., Ltd. operates across medical research, Class I medical devices, rubber and plastic products, and related technical services. It has three production lines, 12 years of combined R&D engineer experience, inventory capability, 100% finished-product inspection, and documented corrective-action and customer-complaint procedures. The supplier provides OEM/ODM-related customization and 3D design services, but reported no new products in the past year. Its manufacturing capacity lacks a valid contract with affiliated subcontractors, and it has no overseas warehouses, agents, branches, showrooms, or offline trade-show participation. Quality assurance is stated as available, while supplier approval records lack signatures or dates. Digital management capability is limited, with no ERP integration and zero reported OA, CRM, or SAP capability. The evidence is insufficient to establish customer cases or formal certification holdings.

Supplier typeThe supplier is identified as a combined company whose scope includes medical research and technical services, Class I medical device production, rubber and plastic manufacturing, and sanitary products. It operates three production lines, indicating an integrated manufacturing and service-oriented profile rather than a purely trading business.

After-Sales capabilityThe supplier has clear procedures and followed records for corrective and preventive actions and customer complaints, supporting internal service-response capability. However, it has no overseas agents or branches, no overseas warehouse, no overseas showroom, and reports service coverage in zero countries, limiting demonstrated international after-sales reach.

R&D capabilityThe supplier has 12 years of total R&D engineer experience, offers 3D software design and ODM services, and supports several customization modes. However, it reported no new products during the past year and has no available SDK, so the evidence supports design and development capacity but not strong recent product innovation.

Production capacityProduction capability is supported by three production lines, injection and blow molding equipment, Class I medical device and rubber/plastic manufacturing scope, inventory capability, and 100% finished-product inspection with standardized instructions. A material operational weakness is that the factory and affiliated subcontractors have no valid manufacturing-capacity contract; production digitalization is also limited because ERP, OA, CRM, and SAP capabilities are absent or reported as zero.

Customization capabilityThe supplier explicitly offers 3D software design services and customization from samples, designs, full requirements, minor requirements, and flexible requirements. These capabilities are reported consistently in both R&D and design-service records, indicating broad customization support.