FDA UDI In Commercial Distribution 🇺🇸 United States

Ear Wax Removal Kit

DI: 00714646000675 · Model: 702 · Bionix, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ear Wax Removal Kit
Primary DI
00714646000675
Version / Model
702
Catalog Number
702
Company Name
Bionix, LLC
Labeler DUNS
117844489
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-07-11
Public Version
1
Public Version Date
2024-07-19
Public Version Status
New
Public Device Record Key
196085d8-47bc-499c-9fe7-0a0eb40c78fa

Device Description

Ear Wax Removal Kit

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
Yes
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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LRD APPLICATOR, ENT DRUG

GMDN Terms

Code Name
62863 Ear canal irrigation kit, reusable

Identifiers

Type ID
Primary 00714646000675

Customer Contacts