FDA UDI In Commercial Distribution 🇺🇸 United States

Eclipse Needle

DI: 00382903032785 · Model: 303278 · BECTON, DICKINSON AND COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Eclipse Needle
Primary DI
00382903032785
Version / Model
303278
Catalog Number
303278
Company Name
BECTON, DICKINSON AND COMPANY
Labeler DUNS
001292192
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-11-13
Public Version
2
Public Version Date
2025-12-11
Public Version Status
Update
Public Device Record Key
be63c267-33eb-4a64-9e1b-ab8822e4c36e

Device Description

NEEDLE ECLIPSE 23X1-1/2 RB TW BNS

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
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 50382903032780
Primary 00382903032785

Premarket Submissions

Submission Number Supplement Number
K161170 000

Device Sizes

Type Value Unit Text
Length 1.5 Inch

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