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Nova Plus®

FDA UDI

Class II (US FDA UDI)

by 3m Company

Identity

Trade Name
Nova Plus® FDA UDI
Generic Name
Electrocardiographic electrode, single-use FDA UDI
Device Name
Nova Plus® Foam Monitoring Electrode V2228-3, 3/BAG, 200/CASE, 54/PLT FDA UDI
Model / Reference
V2228-3 FDA UDI
Description
Nova Plus® Foam Monitoring Electrode V2228-3, 3/BAG, 200/CASE, 54/PLT FDA UDI

Identifiers

Catalog Number
V2228-3 FDA UDI
Primary DI / UDI-DI
10707387787629 FDA UDI
FDA Product Code
DRX FDA UDI
GMDN Term
Electrocardiographic electrode, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2360 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrocardiographic electrode, single-use

Nova Plus® by 3m Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic electrode, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3m Company

Sources (1)

  • FDA UDI 81f91fbf-420c-4409-9c52-0703376fed2f 35 fields · synced May 30, 2026