← Back to catalogue

Vital Signs™ Cable for CAM14 for CASE™, 4.6 m/15 ft

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 2016560-002

by AirLife Finland Oy

Identity

Trade Name
Vital Signs™ Cable for CAM14 for CASE™, 4.6 m/15 ft EUDAMED
Vital Signs™ FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
Vital Signs™ Communication Cable EUDAMED
Cable for CAM14, for CASE , 4.6m / 15ft FDA UDI
Model / Reference
2016560-002 EUDAMEDFDA UDI
Description
Cable for CAM14, for CASE , 4.6m / 15ft FDA UDI

Identifiers

Catalog Number
2016560-002 FDA UDI
Primary DI / UDI-DI
10190752179028 EUDAMEDFDA UDI
Basic UDI-DI
0190752TDHEL1411UU EUDAMED
Direct Marketing DI
10190752179028 EUDAMED
FDA Product Code
IKD FDA UDI
EMDN Code
Z12050380 ELECTROCARDIOGRAPHS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Electrical-only medical device connection cable, reusable FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
890.1175 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

Yes

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™ Cable for CAM14 for CASE™, 4.6 m/15 ft by AirLife Finland Oy — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

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 3d74ab13-505b-407c-9bbd-2b0dd5ee1d81 61 fields · synced Jun 19, 2026
  • FDA UDI 6037856c-465f-444a-bb4d-9b09d92a2223 36 fields · synced May 30, 2026