FDA UDI In Commercial Distribution 🇺🇸 United States

NeoBar®

DI: 10812594010993 · Model: Jumbo Hydrocolloid · Neotech Products LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
NeoBar®
Primary DI
10812594010993
Version / Model
Jumbo Hydrocolloid
Catalog Number
N716H
Company Name
Neotech Products LLC
Labeler DUNS
198013435
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2021-06-02
Public Version
4
Public Version Date
2023-09-20
Public Version Status
Update
Public Device Record Key
c9f4773f-2c8f-4a45-bf38-bafcb444e6ef

Device Description

The NeoBar is intended to secure an endotracheal tube. It is intended for use on pediatric (neonates, infants and children) patients.

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
CBH Device, Fixation, Tracheal Tube

GMDN Terms

Code Name
35815 Endotracheal tube holder

Identifiers

Type ID
Unit of Use 00812594010996
Primary 10812594010993