Import Disposable Ear Piercing Unit — Buy in Bulk from Supplier in China

The Disposable ear piercing unit is a single-use medical device combining a spring-loaded piercing gun with an integrated, pre-sterilized ear stud. It is designed to eliminate cross-contamination risks inherent in reusable piercers. Each unit is individually blister-packed and sterilized using ethylene oxide gas, meeting ISO 11135 standards for medical device sterilization. The product is manufactured in a Class 100,000 cleanroom environment to maintain sterility prior to packaging.

The piercing mechanism is mechanically calibrated to deliver consistent force and depth, reducing the risk of tissue trauma. The ear stud is typically made of surgical-grade stainless steel or hypoallergenic polymer, embedded securely within the device to prevent contamination. The sterilization process ensures the elimination of bacterial spores, unlike alcohol-based disinfection, which is ineffective against Clostridium spores and other resilient pathogens. Shelf life is two years from manufacture when stored in dry, ambient conditions.

This product is primarily sourced by beauty salons, tattoo parlors, medical clinics, and retail kiosks in North America, Europe, and Southeast Asia. Buyers prioritize sterility assurance, ease of use, and compliance with local health regulations. The supplier does not specify MOQ or lead time. Packaging is individual blister packs, with bulk cartons containing 100 to 500 units. Custom branding is not mentioned, and no clinical validation data is provided.

Jiangxi 3L Medicial Product Co Ltd is a manufacturer based in Nanchang, Jiangxi, with a registered address in the Gaoxin Development Zone. The supplier is classified as imported-tier and harbor-tier, indicating verified export experience and logistics access. The listing confirms production in a Class 100,000 cleanroom and EO sterilization capability, but provides no information on company history, workforce size, or quality management system certifications such as ISO 13485.

There is no public record of response rate or average reply time. The supplier does not list clinical trial data, regulatory approvals beyond sterilization, or client references. The product description emphasizes safety over technical compliance, suggesting a focus on end-user safety rather than formal regulatory submissions. Buyers must independently validate sterilization batch records and packaging integrity.