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Multi-Link™

FDA UDI

Class II (US FDA UDI)

by Airlife, Inc.

Identity

Trade Name
Multi-Link™ FDA UDI
Generic Name
Radiolucent electrocardiographic lead FDA UDI
Device Name
ECG Leadwire, Radiolucent 12-lead, Grabber, AHA, 150 cm/59 in FDA UDI
Model / Reference
403751-024 FDA UDI
Description
ECG Leadwire, Radiolucent 12-lead, Grabber, AHA, 150 cm/59 in FDA UDI

Identifiers

Catalog Number
403751-024 FDA UDI
Primary DI / UDI-DI
10190752106468 FDA UDI
FDA Product Code
DSA FDA UDI
GMDN Term
Radiolucent electrocardiographic lead FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2900 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Radiolucent electrocardiographic lead

Multi-Link™ by Airlife, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiolucent electrocardiographic lead.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Airlife, Inc.

Sources (1)

  • FDA UDI 1238ef2f-7a81-4aa8-afd0-d2f2ac73fde4 36 fields · synced May 30, 2026