BD Integra 305312

GUDID 50382903053129

NEEDLE INTEGRA 23X1 RB TW

BECTON, DICKINSON AND COMPANY

Hypodermic needle, single-use
Primary Device ID50382903053129
NIH Device Record Key4bcf826b-a778-483f-8237-e153338fce3e
Commercial Distribution StatusIn Commercial Distribution
Brand NameBD Integra
Version Model Number305312
Catalog Number305312
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
GS100382903053124 [Unit of Use]
GS130382903053125 [Primary]
GS150382903053129 [Package]
Contains: 30382903053125
Package: Case [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MEGSYRINGE, ANTISTICK

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 Integra]

50382903053136NEEDLE INTEGRA 22X1-1/2 RB TW
50382903053129NEEDLE INTEGRA 23X1 RB TW
50382903053112NEEDLE INTEGRA 25X1 RB TW
50382903053105NEEDLE INTEGRA 25X5/8 RB TW
50382903052832SYRINGE INTEGRA 3ML LL
50382903052757NEEDLE INTEGRA 18X1-1/2 BLUNT FILL
50382903052740SYRINGE INTEGRA 3ML W/NDL 21X1-1/2 RB TW
50382903052733SYRINGE INTEGRA 3ML W/NDL 21X1 RB TW
50382903052726SYRINGE INTEGRA 3ML W/NDL 22X1-1/2 RB
50382903052719SYRINGE INTEGRA 3ML W/NDL 23X1 RB
50382903052702SYRINGE INTEGRA 3ML W/NDL 25X1 RB
50382903052696SYRINGE INTEGRA 3ML LL W/NDL 25X5/8 RB

Trademark Results [BD Integra]

Mark Image

Registration | Serial
Company
Trademark
Application Date
BD INTEGRA
BD INTEGRA
78073776 2783108 Live/Registered
Becton, Dickinson and Company
2001-07-13
BD INTEGRA
BD INTEGRA
76404046 2780487 Live/Registered
Becton, Dickinson and Company
2002-05-07

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.