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Er-1

FDA UDI

Class II (US FDA UDI)

by Etymotic Research, Inc.

Identity

Trade Name
ER-1 FDA UDI
Generic Name
Auditory stimulator FDA UDI
Device Name
ER1 pair, ER1-21, ER1-14A, ER1-14B-S FDA UDI
Model / Reference
ER-1 System FDA UDI
Description
ER1 pair, ER1-21, ER1-14A, ER1-14B-S FDA UDI

Identifiers

Primary DI / UDI-DI
00846430005020 FDA UDI
510(k) Number
K930553 FDA UDI
FDA Product Code
EWO FDA UDI
GMDN Term
Auditory stimulator 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

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Auditory stimulator

Er-1 by Etymotic Research, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Auditory stimulator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ca0bce71-cf49-4f04-bdeb-ef9e87cf832f 34 fields · synced May 30, 2026