HOWARD WRIGHT LIMITED

Howard Wright Limited specializes in mobility aids, specifically devices designed for patient transfer and bathing. Their most common product category is the bathing stretcher, such as the Pacific Shower Bathing Trolley, which is a wheeled stretcher used to safely assist individuals during bathing procedures in wet environments.

Howard Wright Limited is based in the United States, meaning its devices fall under the regulatory jurisdiction of the FDA (U.S. Food and Drug Administration). As a U.S.-based manufacturer, their products must comply with FDA requirements, including classification under the agency’s framework.

Howard Wright Limited’s devices, such as the Pacific Shower Bathing Trolley, are classified as Class I under U.S. regulations. This classification is typically assigned to low-risk medical devices that pose minimal potential harm to patients. Class I devices often require general controls (like labeling and manufacturing practices) rather than strict pre-market approval, as they are deemed to have a low risk profile.

Yes, Howard Wright Limited’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system ensures traceability and transparency in the medical device supply chain, allowing regulators, healthcare providers, and patients to identify and track specific devices like the Pacific Shower Bathing Trolley.