AccessGUDID - DEVICE: Howard Leight by Honeywell (00033552015215)

GUDID

Device Identifier (DI) Information

Brand Name: Howard Leight by Honeywell
Version or Model: AirSoft
Commercial Distribution Status: In Commercial Distribution
Catalog Number: R-01521
Company Name: SPERIAN HEARING PROTECTION, LLC

Primary DI Number: 00033552015215
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 014982953 *Terms of Use

Device Description: Honeywell AirSoft Corded Multiple-Use Earplugs feature a Noise Reduction Rating of 27. Honeywell AirSoft Corded Reusable Earplugs offer unparalleled hearing protection for shooting in a multiple-use earplug. These earplugs feature a unique, four-flange design that creates a better seal in the ear without that "plugged up" feeling you can get with other earplugs. This can be attributed to the noise-blocking fins, which form low-pressure air pockets in your ear canal. The result is more comfortable, more dependable earplugs. The firm stem and tapered design makes for easy insertion and removal. These earplugs also come with a high-visibility cord and convenient carrying case to help prevent loss or misplacement. This package contains two pairs and a carrying case.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	No
Over the Counter (OTC):	Yes
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
35024	Earplugs, single-use	A device, usually used as a pair, made of rubber or pliable plastic/silicone material intended to be inserted into the outer ear canal for protection against excessive noise levels or water entering the ears when swimming/bathing. This device may be premoulded (preformed) or mouldable. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
EWD	Protector, Hearing (Insert)

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: fb589b95-c24b-4422-800e-444441c10643
Public Version Date: June 10, 2022
Public Version Number: 2
DI Record Publish Date: September 11, 2020