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Multi-Link™ ECG Leadwire, Individual Replacement, Green F, Grabber, IEC, 74 cm/…

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 412680-009

by AirLife Finland Oy

Identity

Trade Name
Multi-Link™ ECG Leadwire, Individual Replacement, Green F, Grabber, IEC, 74 cm/29 in EUDAMED
Multi-Link™ FDA UDI
Generic Name
Electrocardiographic lead set, reusable FDA UDI
Device Name
Multi-Link™ ECG Leadwire, Individual Replacement EUDAMEDFDA UDI
Model / Reference
412680-009 EUDAMEDFDA UDI
Description
Multi-Link™ ECG Leadwire, Individual Replacement FDA UDI

Identifiers

Catalog Number
412680-009 FDA UDI
Primary DI / UDI-DI
10190752180482 EUDAMEDFDA UDI
Basic UDI-DI
0190752TDHEL133P4 EUDAMED
FDA Product Code
DSA FDA UDI
EMDN Code
Z12050380 ELECTROCARDIOGRAPHS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Electrocardiographic lead set, reusable FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
870.2900 FDA UDI
Market of Registration
Finland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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
Sterilization Method
High-level Disinfectant FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Electrocardiographic lead set, reusable

Multi-Link™ ECG Leadwire, Individual Replacement, Green F, Grabber, IEC, 74 cm/… by AirLife Finland Oy — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Similar devices

Also classified as Electrocardiographic lead set, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
AirLife Finland Oy
EUDAMED SRN
FI-MF-000001482

Sources (2)

  • EUDAMED bac705d3-43fa-4305-9943-dbcab4b9b6de 61 fields · synced Jun 18, 2026
  • FDA UDI d52ddb8d-0bd4-4ab6-8cb1-357bef72da56 36 fields · synced May 30, 2026