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3 Lead Integrated ECG Cable ( (MC2 +2 more)

FDA UDI

Class II (US FDA UDI)

by Vasomedical, Inc.

Identity

Trade Name
3 Lead Integrated ECG Cable (Models MC2, TS4 and Lumenair™) FDA UDI
Generic Name
Electrocardiographic lead set, reusable FDA UDI
Device Name
3 Lead Integrated ECG Cable (Models MC2, TS4 and Lumenair™) FDA UDI
Model / Reference
Model Lumenair FDA UDI
Description
3 Lead Integrated ECG Cable (Models MC2, TS4 and Lumenair™) FDA UDI

Identifiers

Catalog Number
V10-0017 FDA UDI
Primary DI / UDI-DI
00817980020887 FDA UDI
510(k) Number
K033617 FDA UDI
FDA Product Code
DRN FDA UDI
GMDN Term
Electrocardiographic lead set, reusable FDA UDI
Models / Variants
MC2 FDA UDI
TS4 FDA UDI
Lumenair™) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5225 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrocardiographic lead set, reusable

3 Lead Integrated ECG Cable ( (MC2 +2 more) by Vasomedical, Inc. — Class II — FDA UDI — listed in FDA GUDID — 3 models — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic lead set, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vasomedical, Inc.

Sources (1)

  • FDA UDI 51dcff36-38ea-4658-a9ce-7a286b83b182 36 fields · synced May 30, 2026