BD Eclipse Needle 303304

GUDID 50382903033046

NEEDLE ECLIPSE 23X1-1/2 RB TW

BECTON, DICKINSON AND COMPANY

Hypodermic needle, single-use
Primary Device ID50382903033046
NIH Device Record Key30a23484-86d3-4009-bd3d-85e45aea74da
Commercial Distribution StatusIn Commercial Distribution
Brand NameBD Eclipse Needle
Version Model Number303304
Catalog Number303304
Company DUNS001292192
Company NameBECTON, DICKINSON AND COMPANY
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Length1.5 Inch
Needle Gauge23 Gauge
Length1.5 Inch
Needle Gauge23 Gauge
Length1.5 Inch
Needle Gauge23 Gauge
Length1.5 Inch
Needle Gauge23 Gauge
Length1.5 Inch
Needle Gauge23 Gauge
Length1.5 Inch
Needle Gauge23 Gauge
Length1.5 Inch
Needle Gauge23 Gauge
Length1.5 Inch
Needle Gauge23 Gauge
Length1.5 Inch
Needle Gauge23 Gauge
Length1.5 Inch
Needle Gauge23 Gauge
Length1.5 Inch
Needle Gauge23 Gauge
Length1.5 Inch
Needle Gauge23 Gauge
Length1.5 Inch
Needle Gauge23 Gauge
Length1.5 Inch
Needle Gauge23 Gauge
Length1.5 Inch
Needle Gauge23 Gauge
Length1.5 Inch
Needle Gauge23 Gauge
Length1.5 Inch
Needle Gauge23 Gauge
Length1.5 Inch
Needle Gauge23 Gauge

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Room Temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Room Temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Room Temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Room Temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Room Temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Room Temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Room Temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Room Temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Room Temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Room Temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Room Temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Room Temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Room Temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Room Temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Room Temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Room Temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Room Temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Room Temperature

Device Identifiers

Device Issuing AgencyDevice ID
GS100382903033041 [Primary]
GS130382903033042 [Package]
Contains: 00382903033041
Package: Shelfpack [100 Units]
In Commercial Distribution
GS150382903033046 [Package]
Contains: 30382903033042
Package: Case [12 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FMINeedle, hypodermic, single lumen

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[50382903033046]

Radiation Sterilization


[50382903033046]

Radiation Sterilization


[50382903033046]

Radiation Sterilization


[50382903033046]

Radiation Sterilization


[50382903033046]

Radiation Sterilization


[50382903033046]

Radiation Sterilization


[50382903033046]

Radiation Sterilization


[50382903033046]

Radiation Sterilization


[50382903033046]

Radiation Sterilization


[50382903033046]

Radiation Sterilization


[50382903033046]

Radiation Sterilization


[50382903033046]

Radiation Sterilization


[50382903033046]

Radiation Sterilization


[50382903033046]

Radiation Sterilization


[50382903033046]

Radiation Sterilization


[50382903033046]

Radiation Sterilization


[50382903033046]

Radiation Sterilization


[50382903033046]

Radiation Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-08-09
Device Publish Date2023-08-01

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