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Neuroline SubdermalNeurology Needle Electrodes
FDA UDIClass II (US FDA UDI)
by Ambu A/S
Identity
- Trade Name
- Neuroline SubdermalNeurology Needle Electrodes FDA UDI
- Generic Name
- Subdermal needle electrode FDA UDI
- Device Name
- Ambu Neuroline Subdermal - White wires only - USA FDA UDI
- Model / Reference
- 74512-150/24W FDA UDI
- Description
- Ambu Neuroline Subdermal - White wires only - USA FDA UDI
Identifiers
- Catalog Number
- 74512-150/24W FDA UDI
- Primary DI / UDI-DI
- 05707480121410 FDA UDI
- FDA Product Code
- IKT FDA UDI
- GMDN Term
- Subdermal needle electrode FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.1385 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 150 Centimeter FDA UDILength — 12 Millimeter FDA UDI
Neuroline SubdermalNeurology Needle Electrodes by Ambu A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 f268d423-733a-451a-a561-f7453eea85c2 38 fields · synced May 30, 2026