FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 30382903033455 · Model: 303345 · BECTON, DICKINSON AND COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
N/A
Primary DI
30382903033455
Version / Model
303345
Catalog Number
303345
Company Name
BECTON, DICKINSON AND COMPANY
Labeler DUNS
124987988
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2016-10-20
Public Version
4
Public Version Date
2019-10-23
Public Version Status
Update
Public Device Record Key
47e3ed2a-9f00-48ca-9e2d-cbecea4752f3

Device Description

CANNULA BLUNT PLASTIC

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
Yes
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
FMI Needle, hypodermic, single lumen

GMDN Terms

Code Name
60538 Luer/Luer linear connector, single-use

Identifiers

Type ID
Package 50382903033459
Primary 30382903033455
Unit of Use 00382903033454

Premarket Submissions

Submission Number Supplement Number
K974363 000