FDA UDI In Commercial Distribution 🇺🇸 United States

Nexus TKO®

DI: 10815879020359 · Model: P4841 · NEXUS MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Nexus TKO®
Primary DI
10815879020359
Version / Model
P4841
Company Name
NEXUS MEDICAL, LLC
Labeler DUNS
169260325
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-12
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
f8034759-b571-41bb-b0c8-5c5263d756a9

Device Description

4" Split Septum T-Site Extension Set with Non-Bonded Nexus TKO®-6P, Slip Luer & Pinch Clamp

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FPA Set, Administration, Intravascular

GMDN Terms

Code Name
12170 Intravenous administration tubing extension set

Identifiers

Type ID
Package 30815879020353
Primary 10815879020359

Customer Contacts