BD Ultra-Fine Micro Pen Needle 320749

GUDID 50382903207492

PEN NDL 32G 6MM 3B TW 100CT US

BECTON, DICKINSON AND COMPANY

Autoinjector needle
Primary Device ID50382903207492
NIH Device Record Key5cec6ca7-d7ac-42ff-bd0b-97d64136f6eb
Commercial Distribution StatusIn Commercial Distribution
Brand NameBD Ultra-Fine Micro Pen Needle
Version Model Number320749
Catalog Number320749
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Dimensions

Needle Gauge32 Gauge
Length6 Millimeter
Needle Gauge32 Gauge
Length6 Millimeter
Needle Gauge32 Gauge
Length6 Millimeter
Needle Gauge32 Gauge
Length6 Millimeter
Needle Gauge32 Gauge
Length6 Millimeter
Needle Gauge32 Gauge
Length6 Millimeter
Needle Gauge32 Gauge
Length6 Millimeter
Needle Gauge32 Gauge
Length6 Millimeter
Needle Gauge32 Gauge
Length6 Millimeter
Needle Gauge32 Gauge
Length6 Millimeter
Needle Gauge32 Gauge
Length6 Millimeter
Needle Gauge32 Gauge
Length6 Millimeter
Needle Gauge32 Gauge
Length6 Millimeter
Needle Gauge32 Gauge
Length6 Millimeter
Needle Gauge32 Gauge
Length6 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100382903207497 [Primary]
GS150382903207492 [Package]
Contains: 00382903207497
Package: Case [12 Units]
In Commercial Distribution
GS180382903207493 [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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