The Dental Hyperlight X-Ray (Model M-L88, brand HDR) is an electric dental X‑ray imaging device designed to produce clear images of teeth and gums for diagnosis and treatment planning. It is a Class I medical instrument with CE quality certification and a stated shelf life of 3 years.
Class I indicates a low‑to‑moderate risk medical device under common regulatory frameworks. It generally requires compliance with applicable safety and labeling rules but typically involves fewer regulatory controls than higher‑risk devices.
Yes. The product description lists CE quality certification, which indicates conformity with relevant European safety, health and environmental protection requirements. You should also follow local regulations for X‑ray equipment use.
The device is electric. Specific voltage, current and plug type requirements are not listed in the summary — request the technical datasheet or contact the supplier to confirm mains specifications and site preparation needs before purchase.
The product page lists selling units as a single item and describes accessories in the product name. Exact accessory contents (e.g., positioning devices, cables, mounts) are not specified here — contact the seller or check the full product packing list for details.
Installation typically requires following the manufacturer's instructions and ensuring proper electrical connections. Professional installation and site readiness checks are recommended to meet safety and radiation shielding requirements. Ask the supplier for an installation manual or on‑site support options.
Yes. The product description states online technical support is available. For details about hours, response times and service scope, confirm with the vendor or authorized distributor.
Routine maintenance usually includes visual inspections, cleaning external surfaces with appropriate non‑abrasive disinfectants, periodic functional checks and calibration as recommended by the manufacturer. Do not immerse the unit in liquids. Obtain the maintenance schedule and cleaning instructions from the user manual or supplier.
A 3‑year shelf life indicates the period the manufacturer guarantees the device or certain components retain expected performance when stored under recommended conditions. Before putting the unit into clinical service after storage, follow the manufacturer's pre‑use checks and, if necessary, request functional testing.
The unit carries CE certification which implies it meets applicable safety standards, but safe use depends on correct operation, shielding and adherence to local radiation protection regulations. Operators should follow dose‑minimization practices, use protective gear and ensure proper training and monitoring.
It should be operated by trained dental professionals or radiography‑qualified staff. Although the product is described as easy to operate, personnel should receive training in device operation, image acquisition protocols and radiation safety.
Yes — it can be used for dental imaging of both adults and children. When imaging pediatric patients, follow pediatric exposure settings, use appropriate shielding and adhere to the ALARA (as low as reasonably achievable) principle to minimize dose.
The product is described as producing high‑quality images for accurate diagnosis. Specific image resolution, output formats and digital interface compatibility are not listed here — request the technical specifications or demo from the supplier to confirm compatibility with your practice management or imaging software.
Warranty and repair policies are not specified in the provided description. Contact the manufacturer or authorized distributor for details on warranty length, coverage, repair services, spare parts availability and service contracts.
Contact an authorized HDR distributor or the seller listed on the product page to request a quote, technical datasheet, live demo or to place an order. Ask about shipping, lead times, installation services and any required regulatory paperwork for your region.
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