MIR Spirodoc
Spiromètre portable à écran tactile avec oxymètre 3D en option : 6MWT, test du sommeil, Holter 24h pour SpO2%
Available Configurations
Spirodoc is available in 3 configurations:
- Spirometer
- Spirometer + Oximeter
- Oximeter
Supported Tests
Spirometry: FVC, CV, FEV1, MEF, Comparison PRE/POST bronchodilator
Oximetry (optional): Spot test (SpO2%, BPM), 6MWT, sleep study, 24h Holter for SpO2%
Key Features
Touchscreen
Touchscreen for rapid data entry.
Multifunctional
In addition to spirometry and spot oximetry tests, Spirodoc also allows for 6MWT, sleep study, and 24h Holter tests with the 3D oximetry option.
3D Oximetry
6MWT, sleep study, 24h Holter for SpO2%. Measures desaturation events during exercise, sleep, and daily activities.
Removable Spirometry Optoelectronic Sensor
Available in Spirometer and Spirometer + Oximeter configurations to facilitate oximetry tests.
Triaxial Accelerometer (with 3D oximeter)
Triaxial accelerometer to record patient movement and position during measurement.
Real-time Test
Display of tests in real-time on the PC.
Pediatric Incentive
Real-time animation available on MIR Spiro software for better patient collaboration during the test.
Integrated Temperature Sensor
Automatic BTPS conversion.
Long-lasting Rechargeable Battery
Long-lasting rechargeable lithium battery for extended autonomy in standalone mode.
Theoretical Values
Wide selection of theoretical values, including GLI, ERS, and others, directly on the device and in PC mode.
EMR/DMP Connectivity
Integration via MIR Spiro software with EMR/DMP (on HL7, GDT, FHIR, EXCHANGE PROTOCOL).
Compatible Turbines
| Mouthpiece | Turbine Disinfection | Turbine Calibration | Packaging | Antiviral Filter | |
|---|---|---|---|---|---|
| Disposable Turbine FlowMIR® | Disposable mouthpiece included | Not required | Not required | Individual packaging: per 60 | Optional |
| Reusable Turbine | Not included | Required | Required | 1 unit packaging | Recommended per ATS |
Operating Mode
Spirodoc operates in standalone mode and connected to a PC via USB cable.
MIR Spiro Software
- Complete Spirometry and Oximetry software
- Designed for integration with EMR/DMP
- Compliant with the latest ATS/ERS recommendations
- Available for desktop and portable computers
- macOS and Windows
All MIR professional devices work with MIR Spiro software, the latest generation software for Spirometry and Oximetry.
Platinum Card
To subscribe to a Platinum subscription, you need to have the MIR Spiro Platinum Card.
*Provided with all MIR professional devices, sold online (mymir.spirometry.com) or from your MIR dealer.
Measured Parameters
Spirometry (via MIR Spiro software or standalone device)
| Parameters | Via MIR Spiro Software | Standalone Device |
|---|---|---|
| Spirometry | FVC, VEMS, FEV1, MEF, DEM25-75, TEF, VEMS/CVF, VEM6, VEMS/VEM6, DEM25, DEM50, CVIF, VEMS/CV, ELA, VVM(cal), Temp for DEP, VEM0.5, VEM0.5/CVF, VEM0.75, VEM0.75/CVF, DEM75–85, Extr. Vol, CV, CEV, CVI, CI, CV, VRE VEM3, VIM1, ratio VIM1/CIV, PIF, VEM3/CVF, PIF, VEM2, VEM2/CVF, FIF25, FIF50, FIF75, R50, VEMS/DEP (EI), VEMS/VEM0.5 (VEFI), VT, EV, FR, tl | *FVC, *VEMS, *DEP, CVF, VEMS, VEMS/CVF, VEMS/CV, DEP, T-DEP, DEM25-75, DEM75-85, DEM25, DEM50, DEM75, VEM0.5, VEM0.5%, VEM0.75, VEM0.75%, VEM2, VEM2%, VEM3, VEM3/CVF, VEM6, VEM6%, TEF, VEA, CVIF, VIM1, ratio VIM1/CIV, PIF, FIF25, FIF50, FIF75, R50, VVM cal, CV, CEV, CVI, CI, VRE, VT, EV, FR, tl, tE, VT/tl, tl/tTotal, VVM, ELA *best values |
| Oximetry (optional) | SpO2% [Basal, Min, Max, Moy], BPM [Basal, Min, Max, Moy], T Total, T Analyse, T<90%, T<89%, T<88%, T<87%, EvSpO2%<89, Δ Index, t<40BPM, t>120BPM, Ev<40BPM, Ev>120BPM, SpO2% Fin, BPM Fin, SpO2% Début, BPM Début, T Basal, T Marche, T Récupération, Distance, T2%Δ SPO2, T4%Δ SPO2, Théorique, Théorique min, % Théorique, % Théorique min, AUC/Distance*, Dyspnée début, Dyspnée fin, Dyspnée CHG, Fatigue début, Fatigue fin, Fatigue CHG, Diastolique Début, Systolique Début, Diastolique Fin, Systolique Fin, Pas, VMU**, O2-GAP***, O2, ODI, Durée Moyenne Désat., Tot Désatur., Durée max, Pic Désatur., BPM Index, Désat. moyenne, Chute moyenne, Chute Max, BPM Variation, NOD4%, NOD89%, NOD90%, t.NOD4%, t.NOD89%, t.NOD90% | SpO2% [Basal, Min, Max, Moy], BPM [Basal, Min, Max, Moy], T Total, T Analyse, T<90%, T<89%, T<88%, T<87%, EvSpO2%<89, Δ Index, t<40BPM, t>120BPM, Ev<40BPM, Ev>120BPM, SpO2% Fin, BPM Fin, SpO2% Début, BPM Début, T Basal, T Marche, T Récupération, Distance, T2%Δ SPO2, T4%Δ SPO2, Théorique, Théorique min, % Théorique, % Théorique min, AUC/Distance*, Dyspnée début, Dyspnée fin, Dyspnée CHG, Fatigue début, Fatigue fin, Fatigue CHG, Diastolique Début, Systolique Début, Diastolique Fin, Systolique Fin, Pas, VMU**, O2-GAP***, O2, ODI, Durée Moyenne Désat., Tot Désatur., Durée max, Pic Désatur., BPM Index, Désat. moyenne, Chute moyenne, Chute Max, BPM Variation, NOD4%, NOD89%, NOD90%, t.NOD4%, t.NOD89%, t.NOD90% |
Technical Specifications
| Component | Specification | Parameter | Specification |
|---|---|---|---|
| Main Body | Dimensions: 48 x 101 x 16 mm Weight: 99 g (battery included) |
Turbine | Bidirectional digital turbine |
| Turbine Housing | Dimensions: 47 x 46 x 24 mm Weight: 17 g (battery included) |
Flow Interval | ±16 L/s |
| Turbines | Reusable Turbine (code 910002) Disposable Turbine (code 910004) |
Volume Precision | ±2.5% or 50 ml |
| Accelerometer | Triaxial accelerometer | Flow Precision | ±5% or 200 ml/s |
| Power | 3.7 V Lithium-ion battery, 1100 mAh rechargeable | Dynamic Resistance | <0.5 cm H2O/L/s |
| Current | 1100 mAh | Temperature Sensor | Semiconductor (0-45 °C) |
| Consumption | ~20-30 mA (during test) | Measured Parameters (Spirometry) | FVC, VEMS, VEMS/CVF%, VEM3, VEM3/CVF%, VEM6, VEMS/VEM6%, DEP, DEM25%, DEM50%, DEM75%, DEM25-75%, TEF, VE, ELA, CVIF, VIM1, ratio VIM1/CIV%, PIF, CV, CVI, CEV, CI, VRE, VEMS/CV%, VT, EV, FR, ti, te, ti/tTotal, VVM |
| Battery Charging | Voltage = 5 Vcc, Current = minimum 500 mA, Connector: micro USB type B | Memory Capacity | Over 10000 tests |
| Autonomy | 50 hours | Oximetry (on demand) | |
| Connectivity | USB 2.0, Bluetooth® 2.1 | Measurement Method | Infrared absorption |
| Display | Monochrome LCD, 160 x 80 pixels | SpO2% Range | 0-99% |
| Keyboard | 2.8-inch touchscreen | SpO2% Precision | ± 2% between 70 and 99% SpO2 |
| Mouthpiece | Ø 30 mm (1.18 inch) | Average number of breaths for SpO2 calculation | 8 breaths |
| Type of electrical protection | Internal power supply | Heart Rate Range | 30-254 BPM |
| Safety Level (against electric shock) | Type BF device | Heart Rate Precision | ±2BPM or 2% (whichever is greater) |
| Usage | Continuous use device | Average interval for heart rate calculation | 8 seconds |
| Operating Conditions | Temperature: MIN -20 °C, MAX +60 °C Humidity: MIN 10% HR; MAX 95% HR |
Signal Quality Indication | 0 - 8 segments on screen |
| Storage Conditions | Temperature: MIN +10 °C, MAX +40 °C Humidity: MIN 10% HR, MAX 95 % HR |
Measured Parameters (each test) | SpO2%MIN, SpO2%MEAN, SpO2%MAX, BPM MIN, BPMMEAN, BPM MAX, Ttotal, Tanalysis, T<90%, T<89%, T<88%, T<87%, EvSpO2%<89, Δ Index, T<40BPM, T>120BPM, Ev<40BPM, Ev>120BPM, SpO2%BASE, BPMBASE, ODI, Mean Dur. Desat., TotDesaturat., Longest Desat., Desatur. Peak, BPM Index, Mean Desaturat., Mean Drop, Max Drop, BPM Variation, NOD4%, NOD89%, NOD90%, t.NOD4%, t.NOD89%, t.NOD90% |
| Conditions of Use | Electrical Safety IEC 60601-1 Electromagnetic Compatibility EN 60601-1-2 ISO 80601-2-61:2017 ISO 26782: 2009 ISO 23747: 2015 ATS/ERS: 2005, 2019 (update) IEC 60601-1-6:2010 IEC 60601-1-8:2006+ AMD1:2012 IEC 60601-1-9:2007+AMD1:2013 IEC 62304:2006 + A1:2015 ISO 10993-1:2018 Directive 2014/53/UE RED |
Sleep Test | Body position recording |
6 MWT Test
SpO2% start, SpO2% end, BPM start, BPM end, SpO2% base, Tbaseline, Twalking, Trecovery, Distance, T2%ΔSPO2, T4%ASPO2, Predicted, %Predicted, Predicted min, %Predicted min AUC/Distance, Dyspnea, Dyspnea base, Dyspnea end, Dyspnea CHG, Fatigue base, Fatigue end, Fatigue CHG, Diastolic base, diastolic end, Systolic base, Systolic end, Steps, VMU, O2-GAP, O2 approx. 300 hours of oximetry
Certificates and Registrations
- CE 0476
- FDA 510 (k): K 103530
- Health Canada: 71191 (Class II), 75535 (Class III)
- EMDN Level 4: Z121501
- CND Code: Z12150102 (spiro), Z1203020408 (spiro + oxy)
- GMDN Code: 46906 (spiro), 45607 (spiro + oxy)
- Ministry of Health: 2493989/R (910600), 2494292/R (910606), 2494301/R (910610), 2494198/R (91060011), 2494295/R (9106061), 2494319/R (91061011), 2494380/R (91060010), 2494386/R (91061010)
Recommendations and Conformity Standards
Spirometry: ATS/ERS 2005 + 2019 update; ISO 23747: 2015; ISO 26782: 2009
Oximetry: ISO 80601-2-61:2017
Contact Information
ITALY
MIR Medical International Research S.p.A.
Viale Luigi Schiavonetti, 270 00173, Rome
Tel. +39 06 22 754 777
Fax +39 06 22 754 785
mir@spirometry.com
spirometry.com
USA
MIR USA, Inc.
5462 S. Westridge Drive
New Berlin, WI 53151
Tel. +1 (262) 565-6797
Fax +1 (262) 364-2030
mirusa@spirometry.com
FRANCE
MIR Filiale locale
Jardin des Entreprises, 290, Chemin de Saint-Dionisy
30980 LANGLADE
Tel. +33 (0)4 66 37 20 68
Fax +33 (0)4 84 25 14 32
mirfrance@spirometry.com
BRAZIL
MIR Filiale locale
Rua Pinheiro Machado, 2659, Sl.303, Caxias do Sul RS
Tel. +55 5430253070
mirbrazil@spirometry.com
