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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® Neonatal, Pre-Wired, Radiolucent Monitoring Electrode with Clear Tape, 3/Bag, 30/Box, 300/Case FDA UDI
Model / Reference
V2269T FDA UDI
Description
Nova Plus® Neonatal, Pre-Wired, Radiolucent Monitoring Electrode with Clear Tape, 3/Bag, 30/Box, 300/Case FDA UDI

Identifiers

Catalog Number
V2269T FDA UDI
Primary DI / UDI-DI
30707387770212 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
MRI Safety
MR Conditional 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 7be9c567-ebbc-40bf-94af-7b2af4fc80d1 35 fields · synced Jun 1, 2026