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Vital Signs™ 300-series ECG Care Cable, 5-lead, IEC, 3 m/ 10 ft

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 545301-HEL

by AirLife Finland Oy

Identity

Trade Name
Vital Signs™ 300-series ECG Care Cable, 5-lead, IEC, 3 m/ 10 ft EUDAMED
Vital Signs™ FDA UDI
Generic Name
Electrocardiographic lead set, reusable FDA UDI
Device Name
Vital Signs™ 300-series ECG Care Cable EUDAMED
300-series ECG Care Cable, 5-lead, IEC, 3 m/10 ft FDA UDI
Model / Reference
545301-HEL EUDAMEDFDA UDI
Description
300-series ECG Care Cable, 5-lead, IEC, 3 m/10 ft FDA UDI

Identifiers

Catalog Number
545301-HEL FDA UDI
Primary DI / UDI-DI
10190752181106 EUDAMEDFDA UDI
Basic UDI-DI
0190752TDHEL138PE EUDAMED
Direct Marketing DI
10190752181106 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

Vital Signs™ 300-series ECG Care Cable, 5-lead, IEC, 3 m/ 10 ft 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 01d74887-8336-4519-a9fa-7edfab09a79b 61 fields · synced Jun 18, 2026
  • FDA UDI 4c81fc42-9f3b-4cab-823d-8edaafbdb28c 36 fields · synced May 30, 2026