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 ID: 30382903916604
• NIH Device Record Key: 530a32e6-8f7a-4f22-9d45-2afe4b7d7f87
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Neoflon Pro Safety Safety IV Catheter
• Version Model Number: 391660
• Catalog Number: 391660
• Company DUNS: 124987988
• Company Name: BECTON, DICKINSON AND COMPANY
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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	00382903916603 [Primary]
GS1	30382903916604 [Package]; Contains: 00382903916603; Package: Shelfpack [50 Units]; In Commercial Distribution
GS1	50382903916608 [Package]; Package: Case [4 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K172506

FDA Product Code

• FOZ: Catheter, intravascular, therapeutic, short-term less than 30 days

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: 2018-11-22
• Device Publish Date: 2018-10-22

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

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