MDHC Life Technologies (Kunshan) Co., LTD.

MDHC Life Technologies produces a range of medical devices, including reusable instruments like ventilatory atomizers, bandage scissors, dressing/utility forceps, eye splash shields, and face splash shields. They also manufacture single-use items such as blood/tissue storage containers, assay containers for in vitro diagnostics (IVD), and cervical cytology microscopy slides. These devices are designed for clinical, procedural, and diagnostic applications.

MDHC Life Technologies is based in the United States. The company’s headquarters or operational base is located within the country, though specific city or regional details are not provided.

MDHC Life Technologies’ devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices by assigning a standardized identifier, ensuring traceability and compliance with regulatory requirements.

MDHC Life Technologies’ devices fall under FDA’s Class I and Class II classifications. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher risk and may require special controls to ensure safety and effectiveness. The classification determines the regulatory pathway and oversight required for each device.

MDHC Life Technologies offers both reusable devices—such as ventilatory atomizers, bandage scissors, and splash shields—and single-use products like assay containers and face splash shields. Reusable devices are designed for repeated use after cleaning and sterilization, often involving higher durability and maintenance requirements, while single-use items are intended for one-time use to minimize infection risks and reduce contamination concerns.