BD Neoflon Pro Safety Safety IV Catheter 391660

GUDID 30382903916604

NEOFLON PRO SAFETY 24GX0.75IN STRAIGHT

BECTON, DICKINSON AND COMPANY

Peripheral vascular catheter Peripheral vascular catheter Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula

• 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