How long should I use the product after opening?

After opening and exposure, the product should be used within 6 months.

What should I do if I experience side effects?

If side effects like redness, pain, or irritation occur, stop using immediately and consult a doctor.

What are the payment terms for this product?

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

Children's Scar Removal Gel, 10g - Gentle & Effective Solution for Kids

Name: Children's Scar Removal Gel, 10g - Gentle & Effective Solution for Kids
Brand: Weihai Medison Medical Equipment Co., Ltd,
SKU: 2169853525

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

Children-10g

Trademark

QINGSONGYUHE

Origin

Weihai

Production Capacity

50000PCS/Month

Key features

Gentle & Effective for Kids: Specifically designed 10g gel for treating hypertrophic scars and keloids on children.

ISO Certified Quality: Manufactured under ISO certification standards ensuring high quality and safety.

Biologically Active Dressing: Formulated with polydimethylsiloxane to actively improve scar appearance.

Customized Manufacturing: Product specifications and features are available for customization.

Rapid Off-Season Delivery: Lead time within 15 workdays during off-peak seasons for faster fulfillment.

Global Market Reach: Trusted by customers in North America, Europe, Asia, and South America.

Flexible Payment Terms: Accepts LC, T/T, and Western Union for secure international transactions.

Advanced Production Facility: Produced in a 100,000-level purification workshop with advanced techniques.

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: ≤6.32hTerms 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.