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Nerve Block Plexus Needle Stimulator
US$420.00
10 Pieces

Product profile

Customization

Available

Usage

Anesthesia and Pain Management

Type

Electronic Stimulator

Model NO.

OEM

Licence Number

2001-0264

Specification

17x8.5x4.8 cm

Trademark

HUAXING

Origin

China Jiangsu

Production Capacity

50000PCS/Month

Key features

ISO 13485 Certified: Manufactured in ISO level 8, 7, and 5 clean rooms adhering to GMP standards.
48 Patents Held: Backed by 48 patents and annual $400,000 investment in innovation.
CE Certified Quality: Products certified by TUV Rheinland ensuring international safety standards.
Fast Lead Time: Average lead time within 15 workdays for both peak and off-season.
OEM Service Available: Supports OEM model numbers for customized branding requirements.
Professional QC Team: CFDA certified staff conduct comprehensive raw material and final inspections.

Company profile

Jiangsu Province Huaxing Medical Apparatus Industry Co., Ltd.
Importers and ExportersHigh Repeat Buyers ChoiceExperienced TeamExhibition Experience
Business Type: Manufacturer/Factory, Trading CompanyExport Year: 2011-08-08Nearest Port: ShangHaiAverage Response Time: ≤18hTerms of Payment: LC, T/T, D/P, etc.International Commercial Terms(Incoterms): FOB, CIF, EXW, Others

AI-Powered supplier vetting

SummaryThe supplier demonstrates capabilities in OEM/ODM services, product customization, quality control, and documented research and development processes. It reports CE product compliance certification and has procedures for corrective actions, customer complaints, and finished-product inspection. Production-related evidence includes 10 quality assurance and quality control inspectors, injection molding and ethylene oxide sterilization facilities, and peak-season order fulfillment within 15 workdays. However, the supplier lacks a valid manufacturing-capacity contract with related subcontractors, has no overseas warehouse, no overseas agents or branches, and reports zero countries with overseas services. Export destinations and clinical collaboration in Europe and the Americas are described, but specific customer names or verifiable case details are not provided.
Supplier typeThe supplier appears to be a medical-device manufacturer with its own injection molding and ethylene oxide sterilization facilities, while also offering OEM and ODM services. Its capabilities include inventory service, but manufacturing capacity with related subcontractors is not covered by a valid contract.
CertificationsThe supplier states that its products hold CE compliance certification and that it has another type of sustainable development management system certification. The specific identity and scope of the management-system certification are not provided.
After-Sales capabilityDocumented procedures and records exist for corrective and preventive actions and customer complaint handling, and technical engineers provide production and after-sales technical support. However, the supplier has no overseas agents or branches and reports zero countries with overseas services, limiting demonstrated international service coverage.
R&D capabilityThe supplier reports new products during the past year, provides ODM services, has an available SDK, and maintains documented design inputs, outputs, reviews, verification, and validation materials. Engineers are assigned to customer-request confirmation, technical support, and new product development.
Production capacityProduction evidence includes 10 quality assurance and quality control inspectors, injection molding and ethylene oxide sterilization facilities, standardized finished-product inspection instructions, inventory capability, and peak-season fulfillment within 15 workdays. The absence of a valid contract with related subcontractors is a documented production-capacity governance weakness.
Customization capabilityThe supplier explicitly offers customization from samples, designs, full customization, minor customization, and flexible customization, alongside OEM for well-known brands and ODM services. These statements directly support broad customization capability.

Product Q&A

Q:What certifications does the product have?
A:
The product holds ISO 13485 certification and CE certification by TUV Rheinland.
Q:What is the shelf life of the stimulator?
A:
The shelf life is 3 years.
Q:Can I customize the model number?
A:
Yes, OEM services are available for model numbers.
Q:What is the average lead time for orders?
A:
The average lead time is within 15 workdays for both peak and off-season.
Q:What is the usage of this device?
A:
It is used for anesthesia and pain management.

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