BD Syringe NRFit™ Lok 400182

GUDID 50382904001822

BD® 20mL Syringe NRFit™ Lok

BECTON, DICKINSON AND COMPANY

Neuraxial syringe

• Primary Device ID: 50382904001822
• NIH Device Record Key: 7fd24f30-efc5-4468-9162-e8ec03eca58d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Syringe NRFit™ Lok
• Version Model Number: 400182
• Catalog Number: 400182
• Company DUNS: 001292192
• Company Name: BECTON, DICKINSON AND COMPANY
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00382904001827 [Primary]
GS1	30382904001828 [Package]; Contains: 00382904001827; Package: Shelfpack [48 Units]; In Commercial Distribution
GS1	50382904001822 [Package]; Contains: 00382904001827; Package: Case [4 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K192538

FDA Product Code

• QEH: Piston Syringe with neuraxial connector – epidural, peripheral, and/or indirect cerebral spinal fluid contact

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-03-29
• Device Publish Date: 2022-03-21

On-Brand Devices [BD Syringe NRFit™ Lok]

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