BD Nexiva, BD Q-Syte 383532

GUDID 50382903835329

NEXIVA 22GA 1.00IN Y

BECTON, DICKINSON AND COMPANY

Peripheral vascular catheter

• Primary Device ID: 50382903835329
• NIH Device Record Key: c7d7b563-6686-4b4b-8d84-43a2154093c4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Nexiva, BD Q-Syte
• Version Model Number: 383532
• Catalog Number: 383532
• 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	00382903835324 [Unit of Use]
GS1	30382903835325 [Primary]
GS1	50382903835329 [Package]; Contains: 30382903835325; 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