BPM BPM-ES106 Electrosurgical Unit Ligasure Vessel Sealing

The BPM-ES106 is an electrosurgical unit designed for vessel sealing, cutting and coagulation in ICU, general surgery and clinic settings. It supports monopolar and bipolar modes for a broad range of surgical procedures.

Modes include Pure Cut (standard cutting), Blend 1 (approx. 70% cut/30% coagulation), Blend 2 (approx. 50% cut/50% coagulation), Spray (broad-area hemostasis with shallower penetration), Forced/Porced (fast standard coagulation with moderate thermal penetration) and Bipolar coagulation (gentle localized coagulation with minimal sticking/carbonization).

Pure Cut / Blend 1 / Blend 2 operate at up to 100W, Spray at up to 90W, and Forced and standard bipolar outputs are rated around 60W. Always confirm exact settings on the unit display before use.

Yes. The unit is CE certified and complies with IEC 60601 series safety standards for medical electrical equipment.

The BPM-ES106 is listed as an Instrument Set, Instrument Classification Class II. For local regulatory requirements, confirm with the manufacturer or distributor.

The BPM-ES106 is mains-powered (electric). Check the unit nameplate or user manual for the required input voltage, frequency and fuse specifications before installation.

Yes. The device supports monopolar cutting/coagulation and standard bipolar coagulation. Use only manufacturer‑approved or compatible monopolar return electrodes and bipolar instruments per the user manual.

Only trained medical professionals should operate the unit. Observe standard electrosurgery precautions: verify patient return electrode placement for monopolar use, avoid contact with flammable anesthetics, minimize risk of EMI with nearby monitoring devices, and follow contraindications and warnings in the user manual. Consult hospital policies for patients with implanted electronic devices (e.g., pacemakers).

Typical accessories include monopolar handpieces or pencils, bipolar forceps (e.g., vessel sealing/ligasure instruments), patient return electrodes and compatible leads. Use only manufacturer‑approved or specified accessories; single‑use/disposable items should be discarded per instructions.

Follow the manufacturer's cleaning, disinfection and sterilization instructions in the user manual. Perform routine visual inspections, electrical safety checks and preventative maintenance per the service schedule. Arrange periodic functional and safety testing in accordance with IEC 60601 and local clinical engineering policies.

The product listing indicates a shelf life of 1 year. For storage, keep the unit and accessories in a clean, dry environment within the temperature and humidity ranges specified in the user manual and avoid exposure to corrosive or extreme conditions.

Yes. Operators should receive training on electrosurgery principles, device-specific controls and safety procedures. The manufacturer or distributor can often provide training materials or in-service sessions.

The listed MOQ is 1 piece. Contact the manufacturer, authorized distributor or sales representative for pricing, lead time and ordering procedures.

Warranty terms and service/support packages are not included in the basic product description. Contact the manufacturer or your authorized distributor to obtain warranty details, extended service plans and authorized repair centers.

For technical support, compatibility verification (e.g., instrument/consumable fit) or clinical application guidance, contact BPM or an authorized distributor. Always refer to the official user manual and institution protocols before clinical use.