Identity
- Trade Name
- Disposable cTherm EUDAMEDBRAEBON Disposable cTherm Cannula Thermistor FDA UDI
- Generic Name
- General-purpose patient temperature probe, reusable FDA UDI
- Device Name
- Ultima Airflow Sensor EUDAMEDDisposable thermistor intended for use during sleep disorders studies as a qualitative measure of respiratory airflow for recording onto a data acquisition system. FDA UDI
- Model / Reference
- 0510 EUDAMED0518 EUDAMEDFDA UDI
- Description
- Disposable thermistor intended for use during sleep disorders studies as a qualitative measure of respiratory airflow for recording onto a data acquisition system. FDA UDI
Identifiers
- Catalog Number
- 0518 FDA UDI
- Primary DI / UDI-DI
- B14005180 EUDAMEDFDA UDI
- Basic UDI-DI
- ++B140AirflowRF EUDAMED
- 510(k) Number
- K981445 FDA UDI
- FDA Product Code
- BZQ FDA UDI
- EMDN Code
- Z12100585 POLYSOMNOGRAPHY INSTRUMENTS - CONSUMABLES EUDAMED
- GMDN Term
- General-purpose patient temperature probe, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 868.2375 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Disposable cTherm by Braebon Medical Corporation — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | ++B140AirflowRF | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- BRAEBON Medical Corporation
- EUDAMED SRN
- CA-MF-000002190
- Authorised Representative
- AR Experts B.V. NL-AR-000023989
Sources (2)
- EUDAMED 5ab8313e-eb17-44ba-b734-47b6abfdc4f1 61 fields · synced Jul 9, 2026
- FDA UDI 70c298d6-f133-46a9-b29b-f0332722597e 37 fields · synced May 25, 2026