Farma Sonost 3000

CODE PF1001022

Description

SONOST 3000 is the newest ultrasound devices for bone densitometry measurement QUS (Quantitative Ultrasound)and BMD, (Bone Mineral Density). It provides fast, convenient and easy to use measurements of the calcaneous (heel bone) for superb assessment of osteoporotic fracture risk.
SONOST 3000 is equipped with a display for instant values monitoring. Values can be printed at any time. Measures BQI (Bone Quality Index).
Young adult mean standard variation (T-score)
Age-matched mean standard variation ( Z-score). TECHNICAL SPECIFICATIONS Measurement site: heel bone
Measurement time: less than 15 seconds
Measurement: estimated heel BMD and Bone Quality Index BQI obtained from measured Broadband Ultrasound Attenuation (BUA) and speed of sound (SOS) Estimated index in vivo: SOS (C.V. %) 0,2
BUA (C.V. %) 1,5
BQI (C.V. %) 1,5
Transducer: 25mm-100mm
Separation range: automatic adjustment
Storage capacity: 10.000 patients information
Coupling method: gel coupled )water not used)
Display: 6,4 inch TFT LCD 65.536 colors)
User Interface: Touch screen, keyboard USB (optional), mouse USB (optional)
Printer: thermal printer, external printer (optional)
Power input: AC 100 W – 240 W, 50/60Hz, 130W
Weight: 12 kg
Dimensions: 300x620x390mm

  • cavo alimentazione
  • Manuale d’uso e applicazioni
Applications not available.
Technical features not available.
Accessories
Terapy: Line: Diagnosis Line

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Italian Legislative Decree No. 46 of 24th February 1997, Article 21
1. It is prohibited to advertise to the general public devices that, according to regulations adopted by Ministry of Health decree, may only be sold on prescription or be employed under the supervision of a doctor or other healthcare professional.
2. Advertising to the general public of devices other than those referred to in paragraph 1 are subject to authorization by the Ministry of Health. Opinions on applications for authorization are expressed by the Commission of Experts provided for in Article 6, paragraph 3, of Legislative Decree No. 541 of 30th December 1992, and comprising a representative of the Department of the Ministry of Health responsible for medical devices and a representative of the Ministry of Industry, Trade and Commerce.

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