← Back to catalogue

Vital Signs™ Cardiac Output Care Cable for GE Monitors, 3.6 m/12 ft

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 2025248-001

by AirLife Finland Oy

Identity

Trade Name
Vital Signs™ Cardiac Output Care Cable for GE Monitors, 3.6 m/12 ft EUDAMED
Vital Signs™ FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
Vital Signs™ Cardiac Output Care Cable EUDAMED
Cardiac Output Care Cable for GE Monitors, 3.6 m/12 ft FDA UDI
Model / Reference
2025248-001 EUDAMEDFDA UDI
Description
Cardiac Output Care Cable for GE Monitors, 3.6 m/12 ft FDA UDI

Identifiers

Catalog Number
2025248-001 FDA UDI
Primary DI / UDI-DI
10190752179349 EUDAMEDFDA UDI
Basic UDI-DI
0190752TDHEL1221UM EUDAMED
Direct Marketing DI
10190752179349 EUDAMED
FDA Product Code
MHX FDA UDI
EMDN Code
Z12050580 CARDIAC OUTPUT MEASUREMENT INSTRUMENTS - 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
870.1025 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

Vital Signs™ Cardiac Output Care Cable for GE Monitors, 3.6 m/12 ft by AirLife Finland Oy — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

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 bbb13b55-9bb6-4c8e-b34e-dd50cedfaf5a 61 fields · synced Oct 6, 2026
  • FDA UDI 2a19e4cc-d4a7-4728-b72c-ca3bf37ccb4d 36 fields · synced May 30, 2026