BD Twinpak 303390

GUDID 50382903033909

CANNULA TWINPAK DEVICE

BECTON, DICKINSON AND COMPANY

Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set Medication transfer set
Primary Device ID50382903033909
NIH Device Record Key8b686206-4a08-4be6-8853-c7049e33a03e
Commercial Distribution StatusIn Commercial Distribution
Brand NameBD Twinpak
Version Model Number303390
Catalog Number303390
Company DUNS124987988
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

Customer Support Contacts

Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com
Phone+1(844)823-5433
Emailcustomer_support@bd.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100382903033904 [Unit of Use]
GS130382903033905 [Primary]
GS150382903033909 [Package]
Contains: 30382903033905
Package: Case [10 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 StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-16

On-Brand Devices [BD Twinpak]

50382903033930SYRINGE 10ML LL W/TWINPAK DEVICE
50382903033923SYRINGE 5ML LL W/TWINPAK DEVICE
50382903033916SYRINGE 3ML LL W/TWINPAK DEVICE
50382903033909CANNULA TWINPAK DEVICE

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