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Hotel SPA EVA Sole Slippers Disposable Non Woven Slipper

Name: Hotel SPA EVA Sole Slippers Disposable Non Woven Slipper
Brand: Xiantao Topmed Nonwoven Protective Products Co., Ltd.
SKU: 711263375

Hubei, ChinaXiantao Topmed Nonwoven Protective Products Co., Ltd.

Negotiable

100,000 Pieces

Product profile

Customization

Available

Type

Disposable Medical Supplies

Weight

70g

Model NO.

DFG3

Body Materilal

SBPP

Edge Material

Plastic, Cotton, SBPP, Spunlace

Size

M-L-XL

Application

Hotel, Indoor, Massage Centre

Loading Port

Shanghai/Wuhan

Colors

White, Blue, Green, Pink.Purple

Character

with Toe Open or Close

Feature

Eco-Friendly

Color

White

Age

Adult

Folded

Unfolded

Transport Package

2PCS/Bag, 100PCS/Middle Bag, 1000PCS/CTN

Specification

ISO 13485 and CE certification

Trademark

TOPMED

Origin

Hubei, China

HS Code

6404190000

Production Capacity

5000000PCS/Day

Key features

Eco-Friendly Material: Made of non-woven fabric and EVA, harmless to skin and hygienic.

OEM/ODM Service: Supports customization from samples and designs for brand needs.

ISO13485 Certified: Manufactured under international standards with CE certification.

Fast Delivery: Samples made quickly with fastest delivery dates available.

100% QC Inspection: Strict visual and function inspection before every shipment.

High Capacity: Production capability over 40x40HQ containers per month.

Company profile

High Repeat Buyers ChoiceYears of Export ExperienceExperienced TeamExhibition Experience

Xiantao Topmed Nonwoven Protective Products Co., Ltd.

Hubei, China

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Customization from Samples, Customization from Designs CertifiedExport Year: 16 years CertifiedNearest Port: Shanghai Port.Average Response Time: ≤3.92h

AI-Powered supplier vetting

SummaryXiantao Topmed Nonwoven Protective Products Co., Ltd. is a Chinese manufacturer/factory and group corporation producing licensed Class II medical devices and various industrial textile, plastic, and paper products. It reports ISO 13485, ANSI/ESD, ISO 9001, and GMP certifications, documented corrective-action and complaint-handling procedures, and 11–20 quality-control staff. Manufacturing-related evidence includes sewing and heating-forming facilities, in-stock capability, finished-product inspection instructions, and self-operated import/export rights; however, no valid manufacturing contract with associated subcontractors is reported. The supplier provides customization from samples and designs and has OEM experience with popular brands. Export activity is established, with 16 years of exporting and 90% of total sales from exports. Financial-period information is listed for 2021–2023, but no financial performance details are provided. R&D evidence is limited: total R&D engineer experience is under five...

Supplier typeThe supplier is identified as a manufacturer/factory and group corporation in China, with a limited-company structure. Its stated scope covers production and sales of Class I and Class II medical devices, industrial textiles, plastic products, and paper products, subject to applicable approvals and licenses.

CertificationsThe supplier reports holding ISO 13485, ANSI/ESD, ISO 9001, and GMP management-system certifications. These certifications directly support medical-device quality, general quality management, ESD control, and manufacturing-practice controls.

After-Sales capabilityThe supplier has documented and followed procedures for corrective and preventive actions and customer complaints. However, it reports no overseas agents or branches, no overseas warehouse or showroom, and zero countries listed for overseas services, indicating limited overseas service infrastructure.

R&D capabilityThe supplier reports no available SDK, and total R&D engineer experience is stated as under five years. These facts provide limited evidence of software-development capability and indicate that the available R&D experience is relatively limited; no broader innovation outcomes are provided.

Production capacityProduction capability is supported by the manufacturer/factory status, licensed medical-device production scope, sewing and heating-forming facilities, in-stock capability, standardized finished-product inspection instructions, and 11–20 quality-control staff. A stated weakness is that the factory and associated subcontractors have no valid manufacturing contract.

Customization capabilityThe supplier explicitly provides customization from samples and designs and reports OEM service for popular brands. This directly supports both design-based and sample-based customization, although no details on engineering resources, tooling, or customization limits are provided.