Model NM-F700, with accessories compartment
THE DEVICE COMES EQUIPPED WITH
- Aerosol therapy unit (main unit)
- Power supply cord
- RF8 Plus nebulizer x1
- Child nasal prong x1
- Adults nasal prong x1
- Mouthpiece x2
- Soft Touch adult mask x1
- Soft Touch child mask x1
- Valve x1
- Air filter x2
- Air tube (2 m) x1
GENERAL DESCRIPTION
The innovative product for treatment of the respiratory system diseases and complications. This device is suitable for hospital as well as domestic use. Reliable powerful compressor provides the continuous operation and high speed drug delivery. The compact design allows easy transportation thanks to a comfortable built-in handle. The device is supplied with the RF8 Plus nebulizer equipped with the valve system and a set of comfortable Soft Touch face masks for adults and children. This model is also equipped with the compartment for storing accessories when not in use.
CE marking guarantees high quality and reliability of the device.
INDICATIONS
- The necessity of local therapy for the airways, which appears together with the following diseases: Upper respiratory tract infections (Rhinitis, Pharyngitis, Laryngitis, Tracheitis) and the related complications (Rhinosinusitis, Laryngo tracheitis), acute and chronic bronchitis, bronchial asthma
- Immune system reinforcement
- Post-operative complicaitons prevention
TECHNICAL DATA
| Voltage: | 230 V ~ 50 Hz 140 VA |
| Max pressure: | 2.6 ± 0.4 bar |
| Compressor air output: | 10 l/min approx. |
| Sound level (at 1 m): | Approx. 57 dB (A) with open cover approx. 54 dB (A) with closed cover continuous |
| Dimensions (WxDxH): | 270 x 180 x 110 mm |
| Weight: | 1.7 kg |
RF8 NEBULIZER
| Medication minimum capacity [ml] |
Medication maximum capacity [ml] |
(1) Operating pressure [bar] |
(1) Delivery [ml/min] (approx.) |
(2) MMAD [μm] |
(2) BREATHABLE FRACTIONS < 5 μm (FPF) % |
|||
| 2 | 8 | 1.15 | max 0.44 |
min 0.28 |
max 4.12 |
min 3.69 |
max 59.8 |
min 64.2 |
(1) Values measured according to Manufacturer’s internal procedure I29-P07.5 Delivery rate values can change depending on the patient’s respiratory capacity.
(2) In vitro testing certified by TÜV Rheinland LGA Products GmbH – Germany in compliance with the European Standard EN 13544-1 for nebulising systems. Further details available on request.
