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Spo2 Cable For Medibyte, Large Soft Shell
EUDAMEDFDA UDIClass I (EU MDR)
Ref 8898
Identity
- Trade Name
- SPO2 CABLE FOR MEDIBYTE, LARGE SOFT SHELL EUDAMEDBRAEBON SpO2 Cable for MediByte, Large Soft Shell FDA UDI
- Generic Name
- Pulse oximeter probe, reusable FDA UDI
- Device Name
- SpO2 Cable EUDAMEDSilicon finger probe for measuring blood oxygen saturation. Plugs directly into the MediByte. FDA UDI
- Model / Reference
- 8898 EUDAMEDFDA UDI
- Description
- Silicon finger probe for measuring blood oxygen saturation. Plugs directly into the MediByte. FDA UDI
Identifiers
- Catalog Number
- 8898 FDA UDI
- Primary DI / UDI-DI
- B14088980 EUDAMEDFDA UDI
- Basic UDI-DI
- ++B140SpO2E7 EUDAMED
- Direct Marketing DI
- B14088980 EUDAMED
- 510(k) Number
- K061764 FDA UDI
- FDA Product Code
- MNR FDA UDI
- EMDN Code
- Z12100580 POLYSOMNOGRAPHY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
- GMDN Term
- Pulse oximeter 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
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
Yes
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
Spo2 Cable For Medibyte, Large Soft Shell 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 | ++B140SpO2E7 | 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 10eb7fa2-e4c9-4cc7-81d5-35f161cb0928 61 fields · synced Oct 6, 2026
- FDA UDI 1ca18bd8-4798-43e3-a7cf-7c04a7c5c69c 37 fields · synced May 30, 2026