BD EclipseTM Needle 23G x 1"TW 305826

GUDID 00382903058266

BD EclipseTM Needle 23G x 1"TW

BECTON, DICKINSON AND COMPANY

Hypodermic needle, single-use
Primary Device ID00382903058266
NIH Device Record Keyf04688d3-0c05-42c1-992e-9bf60473c2e8
Commercial Distribution StatusIn Commercial Distribution
Brand NameBD EclipseTM Needle 23G x 1"TW
Version Model Number305826
Catalog Number305826
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

Device Dimensions

Length1 Inch
Needle Gauge23 Gauge
Length1 Inch
Needle Gauge23 Gauge
Length1 Inch
Needle Gauge23 Gauge
Length1 Inch
Needle Gauge23 Gauge
Length1 Inch
Needle Gauge23 Gauge
Length1 Inch
Needle Gauge23 Gauge
Length1 Inch
Needle Gauge23 Gauge
Length1 Inch
Needle Gauge23 Gauge
Length1 Inch
Needle Gauge23 Gauge
Length1 Inch
Needle Gauge23 Gauge
Length1 Inch
Needle Gauge23 Gauge
Length1 Inch
Needle Gauge23 Gauge
Length1 Inch
Needle Gauge23 Gauge
Length1 Inch
Needle Gauge23 Gauge
Length1 Inch
Needle Gauge23 Gauge
Length1 Inch
Needle Gauge23 Gauge
Length1 Inch
Needle Gauge23 Gauge

Device Identifiers

Device Issuing AgencyDevice ID
GS100382903058266 [Primary]

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 Date2023-08-15
Device Publish Date2023-08-07

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