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3M Company dba 3M Health Care

FDA UDI

Class II (US FDA UDI)

by 3m Company

Identity

Trade Name
3M Company dba 3M Health Care FDA UDI
Generic Name
Electrocardiographic electrode, single-use FDA UDI
Device Name
3M™ Red Dot™ ECG Resting Electrodes, 2330, 10 Ea/Card, 10 Card/Bag, 40 Bag/Case FDA UDI
Model / Reference
2330 FDA UDI
Description
3M™ Red Dot™ ECG Resting Electrodes, 2330, 10 Ea/Card, 10 Card/Bag, 40 Bag/Case FDA UDI

Identifiers

Catalog Number
2330 FDA UDI
Primary DI / UDI-DI
10707387817203 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrocardiographic electrode, single-use

3M Company dba 3M Health Care 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 da3361aa-ae98-4590-b39c-f99d76ba6ff0 35 fields · synced May 30, 2026