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

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 545303-HELModel 300 Series ECG Cables

by AirLife Finland Oy

Identity

Trade Name
Vital Signs™ 300-series ECG Care Cable, 5-lead, AHA, 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, 5-lead, AHA, 3 m/ 10 ft FDA UDI
Model / Reference
300 Series ECG Cables EUDAMED
545303-HEL EUDAMEDFDA UDI
Description
Vital Signs™ 300-series ECG Care Cable, 5-lead, AHA, 3 m/ 10 ft FDA UDI

Identifiers

Catalog Number
545303-HEL FDA UDI
Primary DI / UDI-DI
10889483585931 EUDAMEDFDA UDI
Basic UDI-DI
088948320041cECGmon83N EUDAMED
Direct Marketing DI
10889483585931 EUDAMED
510(k) Number
K043572 FDA UDI
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
MRI Safety
MR Unsafe FDA UDI

Category: Electrocardiographic lead set, reusable

Vital Signs™ 300-series ECG Care Cable, 5-lead, AHA, 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

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 fa9b068d-9238-4a16-aac9-64a9e8bb908f 61 fields · synced Jun 19, 2026
  • FDA UDI 0b7dc67c-3479-46ab-9106-c0d0072cb63e 37 fields · synced May 30, 2026