BD EclipseTM Needle 25G x 1"TW 305837

GUDID 00382903058372

BD EclipseTM Needle 25G x 1"TW

BECTON, DICKINSON AND COMPANY

Hypodermic needle, single-use
Primary Device ID00382903058372
NIH Device Record Key7ef13ae7-6999-4028-8844-051abc704bba
Commercial Distribution StatusIn Commercial Distribution
Brand NameBD EclipseTM Needle 25G x 1"TW
Version Model Number305837
Catalog Number305837
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

Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch
Needle Gauge25 Gauge
Length1 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100382903058372 [Primary]
GS130382903058373 [Package]
Package: Pack or Inner Pack [100 Units]
In Commercial Distribution
GS150382903058377 [Package]
Contains: 30382903058373
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 StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-08-15
Device Publish Date2023-08-07

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