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SpiroSphere
EUDAMEDFDA UDIFDA 510(k)Class IIa (EU MDR)
Ref 707406510(k) K173937
Identity
- Trade Name
- SpiroSphere EUDAMEDFDA UDI
- Generic Name
- Diagnostic spirometer, professional FDA UDI
- Device Name
- SpiroSphere EUDAMEDMain Unit of diagnostic spirometer for measurement and data collection of lung function parameters FDA UDI
- Model / Reference
- 707406 EUDAMEDSpiroSphere Main Unit FDA UDI
- Description
- Main Unit of diagnostic spirometer for measurement and data collection of lung function parameters FDA UDI
Identifiers
- Catalog Number
- 707406 FDA UDI
- Primary DI / UDI-DI
- 04057155000771 EUDAMEDFDA UDI
- Basic UDI-DI
- 4057155Z12150101003C7 EUDAMED
- Direct Marketing DI
- 04057155000771 EUDAMED
- 510(k) Number
- K173937 FDA UDI
- FDA Product Code
- BTY FDA UDI
- EMDN Code
- Z12150101 CLINICAL/DIAGNOSTIC SPIROMETERS EUDAMED
- GMDN Term
- Diagnostic spirometer, professional FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 868.1890 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
SpiroSphere by eResearchTechnology GmbH — Class IIa — FDA_510K, MDR — listed in EUDAMED, FDA GUDID, FDA 510(k) — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
United States Active
FDA_510K
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K173937 | Class IIa | Active |
| EUDAMED | European Union | CE/MDR | 4057155Z12150101003C7 | Class IIa | Active |
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Manufacturer
- Manufacturer
- eResearchTechnology GmbH
- EUDAMED SRN
- DE-MF-000008015
Sources (3)
- EUDAMED 3535cd26-953b-4d9f-8618-112ad30cd374 85 fields · synced Jun 18, 2026
- FDA UDI 9c395264-ddc1-4954-aeff-edbf0d2b320b 36 fields · synced May 30, 2026
- FDA 510(k) K173937 1 fields · synced May 18, 2026