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Resonance Impedance R36M PT

440,475.00

Resonance R36M

PRODUCT SPECIFICATIONS

TYMPANOMETRY OPERATING SPECIFICATIONS

PROBE TONE

  • 226 Hz for Admittance (Y) curve tympanometry
  • Probe Tone 226 Hz, 678Hz, 800Hz, 1000Hz

INTENSITY

  • 226 Hz: 85dB SPL ± 2dB
  • Frequency Accuracy: ± 0,5%
  • Harmonic distortion: Less then 1%

ADMITTANCE MEASUREMENTS

  • Compliance range at 226Hz: 0,05 up to 7ml
  • Sensitivity scale: Autoscale to appropriate range; available scale at 226Hz: 1.5, 2, 5ml or 7ml

AIR PRESSURE

  • Control: Automatic and Manual
  • Range: from +400 up to -600 daPa adjustable in 50 daPa steps
  • Pressure accuracy: ±10 daPa or ±10%
  • Sweep rate: 50, 100, 200,300 daPa/sec and automatic
  • Indicator: Measured value is displayed
  • Safety limitations: -800 up to +600 daPa

EUSTACHIAN TUBE FUNCTION

  • ETF test for use with both intact and perforated eardrums
  • Available also test for patulous tympanic membrane

ACOUSTIC REFLEX TESTS

  • Reflex test method: Threshold , Automatic, Manual
  • Stimulus duration: 0,5 , 1 or 2 sec.
  • User selectable protocols for all test methods
  • Ipsi or Contralateral stimulation for all reflex test
  • Automated peak search functions available for all test methods
  • Manual Reflex: Pump manual control of all stimuli
  • Reflex Decay: Threshold , Automatic, Manual
  • Stimulus duration: 10 or 20 sec.
  • ARLT: Threshold , Automatic, Manual
  • Stimulus duration: 1 sec. fixed
  • Non Acoustic: 10/20 sec.

FREQUENCIES AND INTENSITY RANGES

  • Ipsilateral:

– Pure tone level range (dBHL) from 50 to 110

– Noise level range (dBSPL) from 50 to 100

  • Frequency: 500, 1000, 2000, 3000, 4000 Hz, BBN,HP or LP noise
  • Accuracy: ±1%
  • Harmonic distortion (THD): less than 3%
  • Contralateral:

– Pure tone level range (dBHL) from 50 to 120

– Noise level range (dBSPL) from 50 to 115

  • Frequency: 250, 500, 1000, 2000, 3000, 4000, 6000,

8000 Hz, BBN,HP or LP noise

  • Accuracy: ±1%
  • Calibration accuracy ±3 dB

STANDARD ACCESSORIES

  • Headband Probe 226 Hz
  • Probe cleaning tool kit
  • DD45 for Contra
  • Insert for Contra
  • Kit of assorted ear tips; size from 6 mm up to 15 mm
  • Calibration cavity with probe holder
  • Built-in fast thermal printer
  • Thermal paper roll
  • Device dust cover
  • Multilingual Quick user’s handbook
  • Pen Drive
  • Resonance® MDS software with NOAH® module included (demo version)
  • Power supply cable (110 – 220V)
  • Spare fuse

OPTIONALS

  • Kit of assorted silicone ear tips “MS” shape size from 8 mm up to 16 mm
  • External USB Keyboard
  • Carrying bag
  • Foot switch
  • TDH39 for Contra
  • MDS software licence

 

SKU: arphi-resonance-impedance-r36m-pt Category: Tag:

Description

GENERAL SPECIFICATIONS

POWER

CLINICAL MIDDLE EAR ANALYZER

DIMENSIONS AND WEIGHT

  • L x W x H: 370x290x180 mm
  • Net weight: 3.5 kg
  • Body material: Bayblend® self-extinguishing

TEST TYPES

Tympanometry, Acoustic Reflex, Reflex Decay, nr. 3

Quick Test, Acoustic Reflex Latency Test (ARLT), ETF

(Intact, Perforated and Patulous), Special tests

(Growht-DLI and Non acoustic)

DISPLAY

  • 7” TFT Color display

USER INTERFACE

  • Multilingual

PRINTER

  • Built-in fast thermal printer with paper width: 112 mm supplied as standard part

REPORTS

  • Printed on thermal printer
  • .pdf report create directly from the device and stored on USB Pen drive with possibility to add patient data

and tests comments via the USB Keyboard (optional)

  • Data transfer to PC using Resonance Management

Data Suite

“CHILDREN” FEATURE

  • To help keep the child distracted while running screening “Quick Check” a series of animated images

appears on the color display

DATA TRANSFER TO PC

  • Via cable trough USB port

COMMUNICATION PORT

  • Nr.1 USB host type A
  • Nr.1 USB slave type B

WINDOWS® COMPATIBLE SOFTWARE

  • Resonance MDS Management Data Suite

POWER SUPPLY

  • 110-240V AC 50/60Hz 40VA
  • Fuses: 2 x T 1 A L 250V

CONSUMPTION

  • Max current: 0,15A
  • Power consumption: 40VA

ENVIRONMENTAL

OPERATING ENVIRONMENT

  • Storage: -20° C up to +50° C
  • Operating: +15° C up to +35° C
  • Humidity: up to 90%, (non condensing)
  • Ambient pressure: from 700hPa up to 1060hPa

QUALITY SYSTEM

Manufactured, designed, developed and marketed

under an ISO 13485, ISO 9001 certified quality system.

Medical CE mark and FDA approval.

COMPLIANCE/REGULATORY

STANDARDS

Designed, tested and manufactured to meet the

European and International Standards:

  • MDD 93/42/EEC and update 2007/47/CEE:

Class IIa (as referred to in Annex IX, rule 10 of said

MDD 93/42 EEC )

  • Safety: IEC 60601-1, 3rd and 2nd edition,

Class 1 Type B

  • EMC: IEC 60601-1-2
  • Impedance: IEC 60645-5/ANSI S.3.39 Type 1

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