FDA UDI In Commercial Distribution 🇺🇸 United States

BD Eclipse, BD Luer-Lok

DI: 00382903033218 · Model: 303321 · BECTON, DICKINSON AND COMPANY
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
BD Eclipse, BD Luer-Lok
Primary DI
00382903033218
Version / Model
303321
Catalog Number
303321
Company Name
BECTON, DICKINSON AND COMPANY
Labeler DUNS
001292192
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-02
Public Version
2
Public Version Date
2024-02-26
Public Version Status
Update
Public Device Record Key
55983d7c-8a19-486c-84e9-64c2dcc8a7aa

Device Description

SYR 10ML 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
FMF Syringe, piston
FMI Needle, hypodermic, single lumen

GMDN Terms

Code Name
63095 General-purpose syringe/needle

Identifiers

Type ID
Package 50382903033213
Package 30382903033219
Primary 00382903033218

Premarket Submissions

Submission Number Supplement Number
K161170 000