BD Syringe NRFit™ Lok 400183

GUDID 50382904001839

BD® 50mL Syringe NRFit™ Lok

BECTON, DICKINSON AND COMPANY

Neuraxial syringe
Primary Device ID50382904001839
NIH Device Record Key9e29573e-ed9a-4e42-b68b-e52dab30facf
Commercial Distribution StatusIn Commercial Distribution
Brand NameBD Syringe NRFit™ Lok
Version Model Number400183
Catalog Number400183
Company DUNS001292192
Company NameBECTON, DICKINSON AND COMPANY
Device Count1
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 Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100382904001834 [Primary]
GS130382904001835 [Package]
Contains: 00382904001834
Package: Shelfpack [40 Units]
In Commercial Distribution
GS150382904001839 [Package]
Contains: 00382904001834
Package: Case [4 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

QEHPiston Syringe with neuraxial connector – epidural, peripheral, and/or indirect cerebral spinal fluid contact

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-03-29
Device Publish Date2022-03-21

On-Brand Devices [BD Syringe NRFit™ Lok]

50382904001839BD® 50mL Syringe NRFit™ Lok
50382904001822BD® 20mL Syringe NRFit™ Lok
30382904001743BD® 10mL Syringe NRFit™ Lok
50382904001730BD® 5mL Syringe NRFit™ Lok
50382904000504BD® 3mL Syringe NRFit™ Lok

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