FDA UDI In Commercial Distribution 🇺🇸 United States

BD Luer-Lok, BD Eclipse

DI: 00382903057849 · Model: 305784 · BECTON, DICKINSON AND COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
BD Luer-Lok, BD Eclipse
Primary DI
00382903057849
Version / Model
305784
Catalog Number
305784
Company Name
BECTON, DICKINSON AND COMPANY
Labeler DUNS
001292192
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
6
Public Version Date
2025-08-01
Public Version Status
Update
Public Device Record Key
d2fd5d93-7015-4653-830f-5f8b0ca19b80

Device Description

SYR 3ML LL W/NDL ECLIPSE 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
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
63095 General-purpose syringe/needle

Identifiers

Type ID
Package 50382903057844
Primary 00382903057849
Package 30382903057840

Premarket Submissions

Submission Number Supplement Number
K010188 000

Device Sizes

Type Value Unit Text
Length 1.5 Inch
Total Volume 3 Milliliter
Needle Gauge 21 Gauge

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Fragile, handle with care
Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight
Type
Special Storage Condition, Specify
Special Conditions
Keep dry