3m™

FDA UDI

Class II (US FDA UDI)

by 3m Company

Identity

Trade Name: 3M™ FDA UDI
Generic Name: Electrode conductive medium FDA UDI
Device Name: 3M™ Defibrulator Pads 2346N FDA UDI
Model / Reference: 2346N FDA UDI
Description: 3M™ Defibrulator Pads 2346N FDA UDI

Identifiers

Catalog Number: 2346N FDA UDI
Primary DI / UDI-DI: 30707387284740 FDA UDI
FDA Product Code: GYB FDA UDI
GMDN Term: Electrode conductive medium FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.1275 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Electrode conductive medium

3m™ by 3m Company — 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: 3m Company

Sources (1)

FDA UDI 83901f6d-6f53-451d-ad3e-d952dbed5612 35 fields · synced Jun 8, 2026