BD Ultra Fine Pen Needle 320745

GUDID 50382903207454

PEN NDL 31G 6MM 3B TW 100CT US

BECTON, DICKINSON AND COMPANY

Autoinjector needle
Primary Device ID50382903207454
NIH Device Record Key4c9bba0b-82b9-48c0-b815-e51173092d3d
Commercial Distribution StatusIn Commercial Distribution
Brand NameBD Ultra Fine Pen Needle
Version Model Number320745
Catalog Number320745
Company DUNS001292192
Company NameBECTON, DICKINSON AND COMPANY
Device Count100
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 Latextrue
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Dimensions

Needle Gauge31 Gauge
Length6 Millimeter
Needle Gauge31 Gauge
Length6 Millimeter
Needle Gauge31 Gauge
Length6 Millimeter
Needle Gauge31 Gauge
Length6 Millimeter
Needle Gauge31 Gauge
Length6 Millimeter
Needle Gauge31 Gauge
Length6 Millimeter
Needle Gauge31 Gauge
Length6 Millimeter
Needle Gauge31 Gauge
Length6 Millimeter
Needle Gauge31 Gauge
Length6 Millimeter
Needle Gauge31 Gauge
Length6 Millimeter
Needle Gauge31 Gauge
Length6 Millimeter
Needle Gauge31 Gauge
Length6 Millimeter
Needle Gauge31 Gauge
Length6 Millimeter
Needle Gauge31 Gauge
Length6 Millimeter
Needle Gauge31 Gauge
Length6 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100382903207459 [Primary]
GS150382903207454 [Package]
Contains: 00382903207459
Package: Case [12 Units]
In Commercial Distribution
GS180382903207455 [Unit of Use]

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 Date2023-10-06
Device Publish Date2023-09-28

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