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Ambu Neuroline Concentric Cable, Lenght of leadwire: 100 cm (39")

FDA UDI

Class II (US FDA UDI)

by Ambu A/S

Identity

Trade Name
Ambu Neuroline Concentric Cable,Lenght of leadwire: 100 cm (39") FDA UDI
Generic Name
Analytical non-scalp cutaneous lead FDA UDI
Device Name
Lead Wire Length: 100 cm (40") Connector: DIN (60130-9) FDA UDI
Model / Reference
1741 FDA UDI
Description
Lead Wire Length: 100 cm (40") Connector: DIN (60130-9) FDA UDI

Identifiers

Catalog Number
1741 FDA UDI
Primary DI / UDI-DI
05707480000029 FDA UDI
FDA Product Code
IKD FDA UDI
GMDN Term
Analytical non-scalp cutaneous lead FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.1175 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 100 Centimeter FDA UDI

Category: Analytical non-scalp cutaneous lead

Ambu Neuroline Concentric Cable, Lenght of leadwire: 100 cm (39") by Ambu A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Analytical non-scalp cutaneous lead.

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 2fcd9298-d0fd-4662-9a48-d3c2361386f6 37 fields · synced May 30, 2026