FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00382903033690 · Model: 303369 · BECTON, DICKINSON AND COMPANY
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00382903033690
Version / Model
303369
Catalog Number
303369
Company Name
BECTON, DICKINSON AND COMPANY
Labeler DUNS
124987988
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
4
Public Version Date
2023-07-13
Public Version Status
Update
Public Device Record Key
00316a6f-290d-4f1b-9346-8b7d88425d8c

Device Description

Threaded Lock Cannula

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
FPA Set, administration, intravascular

GMDN Terms

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

Identifiers

Type ID
Package 50382903033695
Primary 00382903033690
Package 30382903033691

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K011858 000