FDA UDI In Commercial Distribution 🇺🇸 United States

OtoClear® Ear Wax Removal

DI: 00859911004030 · Model: 701 · Bionix, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OtoClear® Ear Wax Removal
Primary DI
00859911004030
Version / Model
701
Catalog Number
701
Company Name
Bionix, LLC
Labeler DUNS
117844489
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-01-07
Public Version
4
Public Version Date
2023-07-18
Public Version Status
Update
Public Device Record Key
38d15560-7bf7-4176-b8ad-6daf90587dae

Device Description

OtoClear Ear Wax Removal

Device Characteristics

Single Use
No
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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KCP SYRINGE, ENT

GMDN Terms

Code Name
65187 Ear canal irrigation tip

Identifiers

Type ID
Primary 00859911004030

Customer Contacts