B Braun Stimuplex HNS 12 Nerve Stimulator + 4892070 Electrode Cable
B. Braun Stimuplex HNS 12 peripheral nerve stimulator supplied with genuine B. Braun Electrode Cable Ref. 4892070.
The unit is battery operated and uses a standard 9 V alkaline battery. The display, controls and operating functions are shown powered on in the photographs.
Included
- 1 × B. Braun Stimuplex HNS 12 Nerve Stimulator
- 1 × B. Braun Electrode Cable Ref. 4892070 for Stimuplex HNS 11 / HNS 12
- Accessories shown in the photographs
Features
- Battery operated – 9 V alkaline battery
- Large LCD display
- Adjustable stimulation current up to 5 mA
- Fine stimulation-current adjustment
- Selectable pulse duration
- 1 Hz / 2 Hz stimulation frequency
- Tissue impedance display
- Visual and audible indicators
- Rotary adjustment control
- Portable handheld design
- Instrument and remote-control connections
Technical Details
- Manufacturer: B. Braun / Stockert GmbH
- Model: Stimuplex HNS 12
- Device Type: Peripheral Nerve Stimulator
- Battery: 9 V
- Supply Current: 6 mA, maximum 8 mA
- Maximum Stimulation Current: 5 mA
- Load Range: 0–12 kΩ
- Maximum Stimulation Voltage: 95 V
- Stimulation Frequency: 1 Hz / 2 Hz
- Electrode Cable: B. Braun Ref. 4892070
- CE Mark: CE 0366
Condition
Used condition with normal cosmetic signs of previous use.
The unit powers on and the display and controls operate as shown in the photographs.
The equipment is supplied in clean condition. Please inspect all photographs carefully as they form part of the description.
DISCLAIMER
All medical items are sold in good, clean and functioning condition unless otherwise stated. Items are not supplied as sterile unless specifically stated.
It is the buyer's responsibility to have the equipment professionally inspected, tested, calibrated and/or serviced as appropriate before clinical use on humans or animals.
NOTE
Regardless of the origin of the equipment, documentation provided, or identification appearing on the equipment, the equipment described and offered here is not being certified, recommended or offered by the seller for any specific clinical application.
The purchaser is responsible for determining the suitability of the equipment for its intended purpose and for ensuring that all required inspection, servicing, calibration and regulatory requirements are met before use.
The purchaser agrees that the seller shall not be held responsible or liable for injuries or damages, whether incidental or consequential, arising from the use or misuse of the equipment. By purchasing this equipment, the purchaser acknowledges and agrees to the terms of this disclaimer.
CE MARKED
The device bears a CE 0366 marking, as shown on the equipment. Buyers should independently confirm that the equipment meets the regulatory requirements applicable to its intended use and jurisdiction.
U.S. FDA NOTICE
The sale of this item may be subject to regulation by the U.S. Food and Drug Administration (FDA) and state and local regulatory agencies.
If the item is subject to FDA regulation, please do not purchase unless you are an authorized purchaser. Where applicable, we may verify the purchaser's status before shipment.
Professional / institutional purchasers are responsible for ensuring compliance with all applicable local regulations before purchase and use.