FDA UDI In Commercial Distribution 🇺🇸 United States

BD Nexiva

DI: 00801741222474 · Model: 393559 · BECTON, DICKINSON AND COMPANY
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
BD Nexiva
Primary DI
00801741222474
Version / Model
393559
Catalog Number
393559
Company Name
BECTON, DICKINSON AND COMPANY
Labeler DUNS
124987988
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-08-17
Public Version
2
Public Version Date
2021-11-15
Public Version Status
Update
Public Device Record Key
c4d38df8-8f03-43cf-89e9-4bb1de06b33a

Device Description

Nexiva 18Gx1.25” Dual Port MaxZero Cue

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
No
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
FOZ Catheter, intravascular, therapeutic, short-term less than 30 days

GMDN Terms

Code Name
64574 Peripheral intravenous cannula

Identifiers

Type ID
Package 20801741222478
Package 10801741222471
Primary 00801741222474

Customer Contacts

Device Sizes

Type Value Unit Text
Length 1.25 Inch
Needle Gauge 18 Gauge