Portable 980nm Wavelength Diode Laser for Dental Therapy Oral Therapy Equipment & Accessory Periodontal Laser Treatment

The Portable 980nm Wavelength Diode Laser (Model Coelas) is a compact dental laser device designed for soft‑tissue surgery, periodontal therapy, endodontic procedures and adjunctive tooth whitening. It uses a 980 nm near‑infrared diode laser source and is intended for professional dental use.

Common applications include soft‑tissue surgery (incisions, frenectomy, gingivectomy), periodontal treatments (debridement, bacterial reduction), endodontic adjunctive therapy, and as an adjunct for tooth whitening. Specific indications should follow clinical protocols and practitioner training.

The device must be operated only by licensed dental professionals who have received appropriate training in dental laser safety and clinical protocols. Local regulations may require additional certification.

Yes. Because 980 nm is near‑infrared and not visible to the eye, everyone in the treatment area must wear laser‑rated protective eyewear that is appropriate for the 980 nm wavelength. Follow the manufacturer's eyewear specifications.

The listing indicates the product is classified as a Class II medical instrument under the supplier/manufacturer classification. This generally implies moderate risk and the need for specific regulatory controls. For laser‑specific hazard class (which governs signage and controls), refer to the device documentation or contact the manufacturer.

Yes — the product specification indicates CE quality certification. CE marking means the manufacturer declares conformity with applicable European directives for safety and performance; check the Declaration of Conformity and labeling for the exact scope.

The device is electrically powered. Exact input voltage and power requirements are provided in the user manual and on the device nameplate — verify compatibility with your clinic mains supply and any local electrical standards prior to use.

The unit is described as lightweight and portable for easy handling and transport. The single package dimensions are 50 x 40 x 25 cm and the gross weight is about 10.3 kg. Actual device size and carrying case may vary by configuration.

The product comes with a 2‑year return and replacement service per the listed specification. For full warranty details, terms, what is covered/excluded, and service procedures, contact the supplier or consult the warranty documentation supplied with the product.

A 5‑year shelf life indicates the manufacturer recommends the product or its packaged consumable lifespan for up to five years under proper storage conditions. This does not replace routine maintenance or checks before clinical use.

Typical accessories include handpieces or fiber delivery tips, patient and staff protective eyewear, footswitch, power cords and a user manual. Some tips may be single‑use while others are autoclavable — confirm with the manufacturer/supplier for exact included items and recommended consumables.

Follow the manufacturer’s infection control and cleaning instructions. Non‑autoclavable external surfaces are usually wiped with approved disinfectants; handpieces and fiber tips may be autoclavable or single‑use depending on design. Never expose electrical components to sterilization processes unless specified.

Clinical contraindications and precautions depend on the procedure and patient status. Exercise caution in pregnancy, patients with implanted electronic devices (e.g., pacemakers), or on photosensitizing medications — consult clinical guidelines and the device manual, and obtain medical clearance when needed.

Contact the manufacturer or your authorized distributor for training courses, official replacement parts (fiber tips, handpieces, consumables), maintenance and technical support. Ensure any training covers safe use, laser protocols and emergency procedures.