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Multi-Link™ X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 3-L…

EUDAMED

Class I (EU MDR)

Ref 2090201-621

by AirLife Finland Oy

Identity

Trade Name
Multi-Link™ X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 3-Lead Set for Mindray, Snap, IEC EUDAMED
Device Name
Multi-Link™ X2 Single-Patient-Use Long ECG Leadwire Set EUDAMED
Model / Reference
2090201-621 EUDAMED

Identifiers

Primary DI / UDI-DI
10190752183179 EUDAMED
Basic UDI-DI
0190752TDHEL1312UR EUDAMED
EMDN Code
Z12050385 ELECTROCARDIOGRAPHS - CONSUMABLES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

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

Category: Electrocardiographic lead set, reusable

Multi-Link™ X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 3-L… by AirLife Finland Oy — Class I — MDR — listed in EUDAMED

Similar devices

Also classified as Electrocardiographic lead set, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
AirLife Finland Oy
EUDAMED SRN
FI-MF-000001482

Sources (1)

  • EUDAMED d3e09635-a1fb-4fbc-a44f-3931a8d81030 61 fields · synced Jun 18, 2026