FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 30382903051909 · Model: 305190 · BECTON, DICKINSON AND COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
N/A
Primary DI
30382903051909
Version / Model
305190
Catalog Number
305190
Company Name
BECTON, DICKINSON AND COMPANY
Labeler DUNS
001292192
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2016-09-16
Public Version
5
Public Version Date
2019-10-23
Public Version Status
Update
Public Device Record Key
810295e1-144f-47a9-81a1-fd4135781068

Device Description

NEEDLE 21X1-1/2 RB TW

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
59230 Hypodermic needle, single-use

Identifiers

Type ID
Package 50382903051903
Primary 30382903051909
Unit of Use 00382903051908

Premarket Submissions

Submission Number Supplement Number
K021475 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Room Temperature