How long is the lead time?

Peak season lead time is one month; off-season is within 15 workdays.

What are the payment terms?

We accept LC, T/T, and Western Union.

Is the product sterilized?

Yes, it undergoes Ethylene Oxide Sterilization.

Reliably Safe Disposable Anastomosis Stapler for Male Circumcision

Name: Reliably Safe Disposable Anastomosis Stapler for Male Circumcision
Brand: Weihai Medison Medical Equipment Co., Ltd,
SKU: 2184028835

Shandong, ChinaWeihai Medison Medical Equipment Co., Ltd,

US$16.30

1 Piece

Sample price:US$18.00/piece.Request sample

Product profile

Customization

Available

Type

Surgical Stapler

Application

Anorectal, Urology

Material

Stainless Steel,Plastic

Feature

Disposable

Group

Adult,Children

Ethylene Oxide Sterilization

Logo

Medison,OEM,ODM

Usage

Hospital Medical

Place of Origin

China

MOQ

1 Piece

Transport Package

Carton

Specification

12, 16, 22, 26, 30, 36

Trademark

Medison, ODM, OEM

Origin

Weihai China

Production Capacity

500000

Key features

Disposable Design: Prevents cross-infection during surgery with single-use construction.

Pain Reduction: Smooth incision edges and quick recovery minimize patient discomfort.

Integrated Cutting: Combines cutting and suturing to shorten operation time significantly.

No Foreign Body: Seamless thread ligation avoids residue and foreign body discomfort.

Multi-Size Options: Available in models MDCS-A-12, 16, 22, 26, 30, and 36 for various needs.

OEM/ODM Service: Custom logo printing available for Medison, OEM, and ODM clients.

Ethylene Oxide Sterilization: Ensures high-level sterility for safe clinical application.

Low MOQ: Minimum order quantity starts from just 1 piece.

Company profile

Importers and ExportersHigh Repeat Buyers ChoiceYears of Export ExperienceSelf-branded

Weihai Medison Medical Equipment Co., Ltd,

Shandong, China

Business Type: Manufacturer/FactoryExport Year: 2003-01-23Nearest Port: QINGDAOAverage Response Time: ≤7.46hTerms of Payment: LC, T/T, Western UnionInternational Commercial Terms(Incoterms): FOB

AI-Powered supplier vetting

SummaryThe supplier is a combined company with licensed activities covering Class II and Class III medical-device production, disinfection-product production, and Class III medical-device operations. It demonstrates documented procedures for quality assurance, corrective and preventive actions, complaint handling, finished-product inspection, and supplier-service assessment. The supplier holds ISO 9001:2015 certification and reports three R&D engineers, recent new-product development, 3D design services, and broad customization capabilities. It has 21 years of export experience, self-operated import/export rights, and customers in several overseas markets. However, the available information shows no in-stock capability, overseas warehouse, overseas showroom, or valid manufacturing-capacity contract with a related subcontractor. Financial credibility and specific customer case details cannot be fully assessed from the provided information.

Supplier typeThe supplier is identified as a combined company. Its stated licensed scope includes production of Class II and Class III medical devices, disinfection products, and operation of Class III medical devices, while its general scope also includes Class I and Class II medical-device sales and related technical services.

CertificationsThe supplier reports holding an ISO 9001:2015 certificate and other certifications. The available information confirms certification is held, although the specific additional certifications are not identified.

After-Sales capabilityThe supplier has documented and followed procedures for corrective and preventive actions and customer complaint handling, and it has overseas agents or branches. However, it reports no overseas warehouse, showroom, or in-stock service capability, so physical overseas support resources are limited.

R&D capabilityThe supplier reports new products within the past year, 3D software design services, three R&D engineers, and a stated focus on technical innovation in medical devices. These points provide explicit evidence of active product-development capability.

Production capacityThe supplier has licensed production activities for Class II and Class III medical devices and disinfection products, applies uniform finished-product inspection instructions, and reports average lead times within 15 workdays in both peak and off-season. Nevertheless, it has no in-stock capability and no valid manufacturing-capacity contract with a related subcontractor, so capacity depth is not fully demonstrated.

Customization capabilityThe supplier explicitly offers customization from samples, customization from designs, full customization, minor customization, and flexible customization. It also provides 3D software design services, indicating support for both design-led and sample-led customized development.