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Kamplex
Kamplex R16M-D Diagnostic Tympanometer Middle Ear Analyzer ETF Reflex Decay
1,999 GBP ex. VAT + shipping
● In stock · 1
Included in this sale
Technical specifications
Full product description
Kamplex R16M-D Diagnostic Tympanometer Middle Ear Analyzer ETF Reflex Decay with
Probe Printer & Dock
Kamplex R16M-D portable tympanometer / middle-ear analyser for audiology and ENT assessment. Supplied with a wired handheld probe, portable thermal printer, docking station, test cavities and UK-plug power adapter as pictured.
Condition
Used, with cosmetic marks from previous use and storage. The unit powers on and displays the operating interface and system information screen.
Included in this sale
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1× Kamplex R16M-D tympanometer
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1× Handheld probe with attached cable
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1× Docking station
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1× Portable thermal printer
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1× UK-plug power adapter
The buyer will receive exactly the items shown in the photos. Please review all photos for the cosmetic condition and included parts.
Technical Specifications
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Brand: Kamplex
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Model: R16M-D
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Product number: 4300105110
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Manufacturer shown on screen: M.R.S. Srl, made for Intricon UK Ltd / PC Werth
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Equipment type: Portable tympanometer / middle-ear analyser
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Display: Colour touchscreen
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Probe: External wired handheld probe
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Firmware version: 2.01
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Software version: 2.01
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Test cavity volumes: 0.5 ml, 2 ml and 5 ml
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Displayed calibration expiry: 10/03/2025
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Printing accessory: Separate portable thermal printer included
Shipping & Returns
Dispatch within 1 working day after payment clears. Worldwide tracked shipping via UPS, DHL, FedEx, Royal Mail or Parcelforce.
14-day return policy. The buyer pays return postage. The item must be returned in its original condition and packaging, with all accessories.
DISCLAIMER: The condition and testing status of this equipment are as stated above. The buyer is responsible for having the equipment professionally tested, calibrated or serviced as required before clinical use on humans or animals.
USE AND RESPONSIBILITY: The seller does not independently certify the equipment’s suitability for a particular clinical application. The purchaser is responsible for checking its suitability and following the manufacturer’s instructions. To the extent permitted by law, the seller accepts no liability for injury or damage arising from improper use. Nothing in this disclaimer excludes or limits liability that cannot legally be excluded or limited, or affects the purchaser’s statutory rights.
CE MARKING: Any CE marking, conformity information and device classification are specific to the product. Please refer to the manufacturer’s label, documentation and information provided in the individual listing.
U.S. BUYERS: The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state or local regulatory agencies. Where purchase restrictions apply, please purchase only if you are authorised to do so. We will verify any required purchaser authorisation before shipping.