BD Eclipse 305759

GUDID 50382903057592

NEEDLE ECLIPSE 25X5/8

BECTON, DICKINSON AND COMPANY

Hypodermic needle, single-use
Primary Device ID50382903057592
NIH Device Record Key024f5df3-0cf0-4127-aea2-89ab43526967
Commercial Distribution StatusIn Commercial Distribution
Brand NameBD Eclipse
Version Model Number305759
Catalog Number305759
Company DUNS001292192
Company NameBECTON, DICKINSON AND COMPANY
Device Count100
DM Exempttrue
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 Identifiers

Device Issuing AgencyDevice ID
GS100382903057597 [Unit of Use]
GS130382903057598 [Primary]
GS150382903057592 [Package]
Contains: 30382903057598
Package: Case [12 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 StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-10-23
Device Publish Date2016-09-16

On-Brand Devices [BD Eclipse]

50382903057691NEEDLE ECLIPSE 23X1-1/4 RB
50382903057684NEEDLE ECLIPSE 22X1 RB
50382903057677NEEDLE ECLIPSE 25X1-1/2 RB
50382903057660NEEDLE ECLIPSE 18X1-1/2 RB
50382903057653NEEDLE ECLIPSE 21X1-1/2 RB TW
50382903057646NEEDLE ECLIPSE 21X1 RB TW
50382903057639NEEDLE ECLIPSE 22X1-1/2 RB
50382903057622NEEDLE ECLIPSE 23X1 RB
50382903057615NEEDLE ECLIPSE 25X1 RB
50382903057592NEEDLE ECLIPSE 25X5/8
50382903057585NEEDLE ECLIPSE 27X1/2
50382903057578NEEDLE ECLIPSE 30X1/2

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