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Neuroline InojectNeurology Needle Electrodes
FDA UDIClass II (US FDA UDI)
by Ambu A/S
Identity
- Trade Name
- Neuroline InojectNeurology Needle Electrodes FDA UDI
- Generic Name
- Electromyographic needle electrode, single-use FDA UDI
- Device Name
- Neurology needle electrodes FDA UDI
- Model / Reference
- 74425-30/10 FDA UDI
- Description
- Neurology needle electrodes FDA UDI
Identifiers
- Catalog Number
- 74425-30/10 FDA UDI
- Primary DI / UDI-DI
- 05707480023813 FDA UDI
- FDA Product Code
- IKT FDA UDI
- GMDN Term
- Electromyographic needle electrode, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.1385 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 25 Millimeter FDA UDILumen/Inner Diameter — 0.3 Millimeter FDA UDI
Category: Electromyographic needle electrode, single-use
Neuroline InojectNeurology Needle Electrodes by Ambu A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Electromyographic needle electrode, single-use.
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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 |
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Manufacturer
- Manufacturer
- Ambu A/S
Sources (1)
- FDA UDI e8a3379f-8c2d-4278-a8d6-5f6c73586512 37 fields · synced Jun 8, 2026