BD Neoflon Pro Safety Safety IV Catheter 391660

GUDID 30382903916604

NEOFLON PRO SAFETY 24GX0.75IN STRAIGHT

BECTON, DICKINSON AND COMPANY

Peripheral vascular catheter
Primary Device ID30382903916604
NIH Device Record Key530a32e6-8f7a-4f22-9d45-2afe4b7d7f87
Commercial Distribution StatusIn Commercial Distribution
Brand NameBD Neoflon Pro Safety Safety IV Catheter
Version Model Number391660
Catalog Number391660
Company DUNS124987988
Company NameBECTON, DICKINSON AND COMPANY
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
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 Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100382903916603 [Primary]
GS130382903916604 [Package]
Contains: 00382903916603
Package: Shelfpack [50 Units]
In Commercial Distribution
GS150382903916608 [Package]
Package: Case [4 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FOZCatheter, intravascular, therapeutic, short-term less than 30 days

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-11-22
Device Publish Date2018-10-22

On-Brand Devices [BD Neoflon Pro Safety Safety IV Catheter]

30382903916635NEOFLON PRO SAFETY 24GX0.75IN WINGED BC
30382903916628NEOFLON PRO SAFETY 24GX0.75IN WINGED
30382903916611NEOFLON PRO SAFETY 24GX0.75IN STR BC
30382903916604NEOFLON PRO SAFETY 24GX0.75IN STRAIGHT

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