← Back to catalogue

Multi-Link™ Single-Patient-Use ECG Leadwire Set 6-LEAD, GRABBER, AHA, 100 cm/39…

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 2086367-003

by AirLife Finland Oy

Identity

Trade Name
Multi-Link™ Single-Patient-Use ECG Leadwire Set 6-LEAD, GRABBER, AHA, 100 cm/39 in EUDAMED
Multi-Link™ FDA UDI
Generic Name
Electrocardiographic lead set, single-use FDA UDI
Device Name
Multi-Link™ Single-Patient-Use ECG Leadwire Set EUDAMEDFDA UDI
Model / Reference
2086367-003 EUDAMEDFDA UDI
Description
Multi-Link™ Single-Patient-Use ECG Leadwire Set FDA UDI

Identifiers

Catalog Number
2086367-003 FDA UDI
Primary DI / UDI-DI
10190752179707 EUDAMEDFDA UDI
Basic UDI-DI
0190752TDHEL1311UP EUDAMED
FDA Product Code
DSA FDA UDI
EMDN Code
Z12050385 ELECTROCARDIOGRAPHS - CONSUMABLES EUDAMED
GMDN Term
Electrocardiographic lead set, single-use 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

Yes

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
MRI Safety
MR Unsafe FDA UDI

Category: Electrocardiographic lead set, reusable

Multi-Link™ Single-Patient-Use ECG Leadwire Set 6-LEAD, GRABBER, AHA, 100 cm/39… 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
AirLife Finland Oy
EUDAMED SRN
FI-MF-000001482

Sources (2)

  • EUDAMED af44e1ad-343d-483b-9d61-fbc20c2c0a82 61 fields · synced Oct 6, 2026
  • FDA UDI da0df6a9-e448-4fb8-9801-7f53d3ef831a 36 fields · synced May 30, 2026