What certifications does the product hold?

The product holds CE, ISO13485, and GMP certifications and meets GB/T 32610 safety standards.

Can the brand be customized?

Yes, OEM services are available, allowing for customized branding on the product.

What is the material of the cannula?

The cannula is made of 304 stainless steel, ensuring durability and reusability.

Nerve Block Needle Ultrasound Guided Regional Anesthesia Block Needle

Name: Nerve Block Needle Ultrasound Guided Regional Anesthesia Block Needle
Brand: Changzhou KEALOR International Co., Ltd.
SKU: 2180310545

Jiangsu, ChinaChangzhou KEALOR International Co., Ltd.

US$4.00-6.00

500 Pieces

Product profile

Customization

Available

Brand Name

Kealor/OEM

Certificate

CE ISO13485 GMP

Model NO.

Nerve Block Needle

Sterilization Method

Co-60 R-Ray Radiation

Shelf Life

2years

Package Type

Sterile Package, Packed by Blister

Length

75/100/150mm

Cannula Material

304

Specification

8g-13G

Trademark

KEALOR

Origin

China

HS Code

9018310000

Production Capacity

500000PCS/Year

Company profile

High Repeat Buyers ChoiceQuality AssuranceRaw-Materials TraceabilityQA/QC Inspectors

Changzhou KEALOR International Co., Ltd.

Jiangsu, China

Business Type: Manufacturer/FactoryExport Year: 2025-02-18Nearest Port: shanghaiAverage Response Time: ≤15hTerms of Payment: LC, T/T, D/P, etc.International Commercial Terms(Incoterms): FOB, EXW, CFR, CIF, DAT, FAS, DDP, DAP, CIP, CPT, Others, FCA

AI-Powered supplier vetting

SummaryKealor presents evidence of established medical and aesthetic manufacturing capabilities, holding ISO 13485, ISO 9001, and GMP certifications, reporting 50 quality-control staff, annual output above the stated threshold, and experience supplying well-known brands. It offers OEM, ODM, and multiple customization options, with raw-material traceability and documented inspection instructions. However, the evidence is inconsistent regarding technical resources: one slice identifies only one R&D engineer and no quality-control test equipment, while another reports 11–20 years of total R&D engineer experience. The supplier lacks 3D software, SDK, overseas warehouses, overseas showrooms, overseas agents or branches, and offline trade-show participation. After-sales technical support is indicated, but formal service-management procedures are absent. Financial records are referenced for several years, but the provided data does not disclose financial performance details. Customer cases are not specifically identified.

Supplier typeThe supplier is explicitly described as not being a professional technical supplier, while its company description focuses on solutions for medical and aesthetic applications. Its certifications and manufacturing indicators support classification as a medical/aesthetic product manufacturer rather than a dedicated technical-services provider.

CertificationsThe supplier reports holding ISO 13485, ISO 9001, and GMP certifications. These explicitly demonstrate certifications covering medical-device quality management, general quality management, and good manufacturing practices.

Production capacityProduction-related evidence includes annual output above the stated threshold, in-stock capability, raw-material traceability, one quality-control inspector, random finished-product inspection, and inspection instructions that are uniformly followed. The supplier has no quality-control test equipment reported in one slice, and manufacturing-contract status is unknown, so production scale is demonstrated but process depth and capacity assurance are only partially evidenced.

Customization capabilityThe supplier explicitly offers customization from samples, customization from designs, full customization, minor customization, and flexible customization, together with OEM and ODM services. These repeated capabilities indicate broad product customization support, despite the absence of 3D software design services.