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Neuroline SubdermalNeurology Needle Electrodes

FDA UDI

Class 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
Needle Electrode Length: 12 mm (0.5") Leadwire Length: 100 cm (40") Each box of 24 consists of 4 pieces in each of the colors: White, Green, Blue, Yellow, Red, Black FDA UDI
Model / Reference
74512-100/24 FDA UDI
Description
Needle Electrode Length: 12 mm (0.5") Leadwire Length: 100 cm (40") Each box of 24 consists of 4 pieces in each of the colors: White, Green, Blue, Yellow, Red, Black FDA UDI

Identifiers

Catalog Number
74512-100/24 FDA UDI
Primary DI / UDI-DI
05707480024162 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 — 100 Centimeter FDA UDI
Length — 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

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Manufacturer

Manufacturer
Ambu A/S

Sources (1)

  • FDA UDI 619bb7c6-33ff-4271-8d91-36b5545f16ef 38 fields · synced Jun 1, 2026