What should I do if I experience side effects?

If you experience skin redness, pain, or irritation, stop using it immediately and consult a doctor.

What is the warranty or return policy?

Please do not use the product if the packaging is damaged. Expired products are prohibited from use.

What are the payment terms?

We accept LC, T/T, and Western Union as terms of payment.

Gentle Scar Gel for Children - Fast Healing Formula

Name: Gentle Scar Gel for Children - Fast Healing Formula
Brand: Weihai Medison Medical Equipment Co., Ltd,
SKU: 2169925125

Shandong, ChinaWeihai Medison Medical Equipment Co., Ltd,

US$3.20

100 Pieces

Sample price:US$3.20/piece.Request sample

Product profile

Customization

Available

Customized

Certification

ISO

Model NO.

Children

Feature

Ventilation

Type

Biologically Active Dressing

Transport Package

Carton

Specification

Child-10g

Trademark

QINGSONGYUHE

Origin

Weihai

Production Capacity

50000PCS/Month

Key features

Fast Healing Formula: Specialized gel for treating hypertrophic scars and keloids on healed wounds.

Child-Specific Design: 10g dosage form tailored for pediatric scar treatment and care.

ISO Certified Quality: Manufactured under ISO certification with advanced clean room techniques.

Customizable Packaging: Customized options available for product specifications and packaging.

Reliable Manufacturer: Established in 2003, specializing in Class I and II medical equipment.

Global Market Reach: Trusted by medical staff in North America, Europe, Asia, and beyond.

Advanced Production: Equipped with first-grade assembly lines and testing equipment.

User-Oriented Innovation: Focus on technical innovation and product function improvement.

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: ≤7.14hTerms 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.