BD Eclipse, BD Luer-Lok 303307

GUDID 30382903033073

SYRINGE 5ML LL 23X1-1/2IN ECLIPSE RB TW

BECTON, DICKINSON AND COMPANY

General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle
Primary Device ID30382903033073
NIH Device Record Keycc4b5f97-bdc9-48d2-bcfa-d41effeb2d24
Commercial Distribution StatusIn Commercial Distribution
Brand NameBD Eclipse, BD Luer-Lok
Version Model Number303307
Catalog Number303307
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

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

Device Identifiers

Device Issuing AgencyDevice ID
GS100382903033072 [Primary]
GS130382903033073 [Package]
Contains: 00382903033072
Package: Shelfpack [50 Units]
In Commercial Distribution
GS150382903033077 [Package]
Package: Case [6 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FMINeedle, hypodermic, single lumen

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-09-13
Device Publish Date2023-09-05

On-Brand Devices [BD Eclipse, BD Luer-Lok]

50382903033213SYR 10ML LL W/NDL ECLIPSE 21X1-1/2 RB TW
30382903033073SYRINGE 5ML LL 23X1-1/2IN ECLIPSE RB TW

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