Vectraplex CMS

FDA UDI

Class II (US FDA UDI)

by Vectracor, Inc.

Identity

Trade Name: Vectraplex CMS FDA UDI
Generic Name: Electrocardiography monitoring system receiver FDA UDI
Device Name: Vectraplex Central Monitoring System FDA UDI
Model / Reference: V100705 FDA UDI
Description: Vectraplex Central Monitoring System FDA UDI

Identifiers

Primary DI / UDI-DI: 00857175006012 FDA UDI
510(k) Number: K140852 FDA UDI
FDA Product Code: MHX FDA UDI
MLD FDA UDI
MSX FDA UDI
GMDN Term: Electrocardiography monitoring system receiver FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.1025 FDA UDI
870.2300 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Electrocardiography monitoring system receiver

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Vectracor, Inc.

Sources (1)

FDA UDI cf38e516-9d31-492a-90f2-d6da60b826da 34 fields · synced May 30, 2026