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VectraplexECG System

FDA UDI

Class II (US FDA UDI)

by Vectracor, Inc.

Identity

Trade Name
VectraplexECG System FDA UDI
Generic Name
Cardiopulmonary physiological parameter analysis software FDA UDI
Device Name
VectraplexECG System with Cardio Electrical Bio-marker (CEB) FDA UDI
Model / Reference
3.4.2 FDA UDI
Description
VectraplexECG System with Cardio Electrical Bio-marker (CEB) FDA UDI

Identifiers

Primary DI / UDI-DI
00857175006029 FDA UDI
510(k) Number
K102378 FDA UDI
FDA Product Code
DPS FDA UDI
MLD FDA UDI
GMDN Term
Cardiopulmonary physiological parameter analysis software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2340 FDA UDI
870.1025 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cardiopulmonary physiological parameter analysis software

VectraplexECG System by Vectracor, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiopulmonary physiological parameter analysis software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vectracor, Inc.

Sources (1)

  • FDA UDI 4e326ac3-c066-4684-b4bc-298effda0ee0 34 fields · synced May 30, 2026