BD Nexiva, BD Q-Syte 383531

GUDID 50382903835312

NEXIVA 24GA 0.75IN Y

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 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 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: 50382903835312
• NIH Device Record Key: ee742717-3211-43d7-b315-e882114a911c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Nexiva, BD Q-Syte
• Version Model Number: 383531
• Catalog Number: 383531
• Company DUNS: 124987988
• Company Name: BECTON, DICKINSON AND COMPANY
• Device Count: 20
• DM Exempt: true
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00382903835317 [Unit of Use]
GS1	30382903835318 [Primary]
GS1	50382903835312 [Package]; Contains: 30382903835318; Package: Case [4 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K102520

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: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-16

On-Brand Devices [BD Nexiva, BD Q-Syte]

• 50382903835404: NEXIVA 18GA 1.75IN HF Y
• 50382903835398: NEXIVA 18GA 1.25IN HF Y
• 50382903835381: NEXIVA 20GA 1.75IN HF Y
• 50382903835374: NEXIVA 20GA 1.25IN HF Y
• 50382903835367: NEXIVA 20GA 1.00IN HF Y
• 50382903835329: NEXIVA 22GA 1.00IN Y
• 50382903835312: NEXIVA 24GA 0.75IN Y
• 50382903835305: NEXIVA 24GA 0.56IN Y