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ABR Electrode Cable (TAB) for OtoNova Pro
FDA UDIClass II (US FDA UDI)
by Otodynamics
Identity
- Trade Name
- ABR Electrode Cable (TAB) for OtoNova Pro FDA UDI
- Generic Name
- Evoked-potential audiometer FDA UDI
- Device Name
- ABR electrode cable for use with TAB electrodes, length 44"/1.1M, Red/Black/White color coding, straight yellow 4-pin plug, for use with OtoNova Pro FDA UDI
- Model / Reference
- NPRO-TEC FDA UDI
- Description
- ABR electrode cable for use with TAB electrodes, length 44"/1.1M, Red/Black/White color coding, straight yellow 4-pin plug, for use with OtoNova Pro FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05060396172366 FDA UDI
- 510(k) Number
- K234095 FDA UDI
- FDA Product Code
- GWJ FDA UDI
- GMDN Term
- Evoked-potential audiometer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.1900 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Category: Evoked-potential audiometer
ABR Electrode Cable (TAB) for OtoNova Pro by Otodynamics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K234095 also covers:
- ABR Electrode Cable (SNAP) for OtoNova Pro — Otodynamics
- Crib/bassinet device holster for OtoNova — Otodynamics
- OtoNova Battery Assembly Service Kit — Otodynamics
- OtoNova Charger — Otodynamics
- OtoNova Pro Case Service Kit — Otodynamics
- OtoNova Pro Charger PCB Service Kit — Otodynamics
- OtoNova Pro Clinical — Otodynamics
- OtoNova Pro Clinical+AABR — Otodynamics
- OtoNova Pro Clinical+TE — Otodynamics
- OtoNova Pro Clinical+TE+AABR — Otodynamics
- OtoNova Pro Fabric Carry Case — Otodynamics
- OtoNova Pro Infection Control Sleeve — Otodynamics
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Otodynamics
Sources (1)
- FDA UDI fd38c1a1-f864-4e8f-8c96-3cc348cee516 35 fields · synced Jun 8, 2026