FDA UDI In Commercial Distribution 🇺🇸 United States

ExT™ Stabilized Extension Set with NearPort™ IV Access

DI: 00382903902200 · Model: 390220 · BECTON, DICKINSON AND COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ExT™ Stabilized Extension Set with NearPort™ IV Access
Primary DI
00382903902200
Version / Model
390220
Catalog Number
390220
Company Name
BECTON, DICKINSON AND COMPANY
Labeler DUNS
124987988
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-12-13
Public Version
1
Public Version Date
2023-12-21
Public Version Status
New
Public Device Record Key
c3448422-b27f-4121-a538-d5f31669e3ee

Device Description

ExT Extension Set - Basic

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 50382903902205
Primary 00382903902200

Premarket Submissions

Submission Number Supplement Number
K200439 000