← Back to catalogue

Howard Leight

FDA UDI

Class U (US FDA UDI)

by Sperian Hearing Protection, Llc

Identity

Trade Name
Howard Leight FDA UDI
Generic Name
Earplugs, single-use FDA UDI
Device Name
Low Pressure Disposable Foam Shooting Earplugs, 10-Pairs FDA UDI
Model / Reference
Leight Plugs FDA UDI
Description
Low Pressure Disposable Foam Shooting Earplugs, 10-Pairs FDA UDI

Identifiers

Catalog Number
R-01518 FDA UDI
Primary DI / UDI-DI
00033552015185 FDA UDI
FDA Product Code
EWD FDA UDI
GMDN Term
Earplugs, single-use FDA UDI

Classification

Device Class
U 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

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Earplugs, single-use

Howard Leight by Sperian Hearing Protection, Llc — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Earplugs, single-use.

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

Sources (1)

  • FDA UDI c98155d7-5fd8-4986-a9d0-37ef3f6e82b8 34 fields · synced May 30, 2026