← Back to catalogue

E-A-Rtone™

FDA UDI

Class II (US FDA UDI)

by 3m Company

Identity

Trade Name
E-A-RTONE™ FDA UDI
Generic Name
Earphone, insert FDA UDI
Device Name
3M(TM) E-A-RTONE(TM) Insert Earphone 3A ABR 50 ohm 410-3018, 1/case FDA UDI
Model / Reference
410-3018 FDA UDI
Description
3M(TM) E-A-RTONE(TM) Insert Earphone 3A ABR 50 ohm 410-3018, 1/case FDA UDI

Identifiers

Catalog Number
410-3018 FDA UDI
Primary DI / UDI-DI
00080529191328 FDA UDI
FDA Product Code
EWO FDA UDI
GMDN Term
Earphone, insert FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.1050 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Earphone, insert

E-A-Rtone™ by 3m Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Earphone, insert.

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
3m Company

Sources (1)

  • FDA UDI 10047253-7b1b-4d9d-b471-f18b47d4e182 35 fields · synced May 30, 2026