FDA UDI In Commercial Distribution 🇺🇸 United States

Howard Leight

DI: 00033552019022 · Model: Impact Pro · SPERIAN HEARING PROTECTION, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
6

Basic Information

Brand Name
Howard Leight
Primary DI
00033552019022
Version / Model
Impact Pro
Catalog Number
R-01902
Company Name
SPERIAN HEARING PROTECTION, LLC
Labeler DUNS
014982953
Distribution Status
In Commercial Distribution
Device Count in Pkg
6
Record Status
Published
Publish Date
2020-07-31
Public Version
1
Public Version Date
2020-08-10
Public Version Status
New
Public Device Record Key
628c9b54-88c8-4b78-89d3-4107919d401f

Device Description

Impact Pro High NRR Sound Amplification Electronic Earmuff, Black & Gray

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EWE Protector, Hearing (Circumaural)

GMDN Terms

Code Name
41232 Acoustic earmuffs

Identifiers

Type ID
Unit of Use 20033552019026
Primary 00033552019022

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
-20C to 60C <90% Humidity