← Back to catalogue

Premier Heart MCG Model VH12

FDA UDI

Class II (US FDA UDI)

by Premier Heart, Llc

Identity

Trade Name
Premier Heart MCG Model VH12 FDA UDI
Generic Name
Electrocardiograph, professional, multichannel FDA UDI
Device Name
Premier Heart MCG 12 Lead capture hardware. FDA UDI
Model / Reference
VH12 FDA UDI
Description
Premier Heart MCG 12 Lead capture hardware. FDA UDI

Identifiers

Primary DI / UDI-DI
B320VH120 FDA UDI
FDA Product Code
DQK FDA UDI
GMDN Term
Electrocardiograph, professional, multichannel FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1425 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

No

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: Electrocardiograph, professional, multichannel

Premier Heart MCG Model VH12 by Premier Heart, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiograph, professional, multichannel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Premier Heart, Llc

Sources (1)

  • FDA UDI 775b3de5-d2c3-4195-bfe9-c813d500c9f1 34 fields · synced May 30, 2026