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EarHug Pack

FDA UDI

Class II (US FDA UDI)

by Intelligent Hearing Systems Corp.

Identity

Trade Name
EarHug Pack FDA UDI
Generic Name
Analytical non-scalp cutaneous electrode FDA UDI
Device Name
25 pair of EarHugs and three packs of Ambu Neuroline (25x) 720 electrodes FDA UDI
Model / Reference
M015402 FDA UDI
Description
25 pair of EarHugs and three packs of Ambu Neuroline (25x) 720 electrodes FDA UDI

Identifiers

Primary DI / UDI-DI
00817020020013 FDA UDI
FDA Product Code
GWJ FDA UDI
GXY FDA UDI
GMDN Term
Analytical non-scalp cutaneous electrode FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1900 FDA UDI
882.1320 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Analytical non-scalp cutaneous electrodeAudiometric ear tip

EarHug Pack by Intelligent Hearing Systems Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Audiometric ear tip.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6aed77b0-e2fe-4dcc-a15b-46bc322f9144 33 fields · synced Jun 8, 2026