FDA UDI In Commercial Distribution 🇺🇸 United States

Eclipse

DI: 00382903058952 · Model: 305895 · BECTON, DICKINSON AND COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Eclipse
Primary DI
00382903058952
Version / Model
305895
Catalog Number
305895
Company Name
BECTON, DICKINSON AND COMPANY
Labeler DUNS
001292192
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-01
Public Version
1
Public Version Date
2023-09-11
Public Version Status
New
Public Device Record Key
6399e4dd-39b3-4af8-abb5-789056d4297c

Device Description

NEEDLE ECLIPSE S/T 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
59230 Hypodermic needle, single-use

Identifiers

Type ID
Package 50382903058957
Package 30382903058953
Primary 00382903058952

Premarket Submissions

Submission Number Supplement Number
K100209 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Room Temperature