BD Introsyte-N, BD Instaflash 384021

GUDID 50382903840217

INTRODUCER INTROSYTE-N 1.9F 1.9CM

BECTON, DICKINSON AND COMPANY

Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable

• Primary Device ID: 50382903840217
• NIH Device Record Key: 18648e85-9080-4c28-8edc-774ce4a29028
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Introsyte-N, BD Instaflash
• Version Model Number: 384021
• Catalog Number: 384021
• Company DUNS: 124987988
• Company Name: BECTON, DICKINSON AND COMPANY
• Device Count: 10
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00382903840212 [Unit of Use]
GS1	50382903840217 [Primary]

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: 2019-06-07
• Device Publish Date: 2016-10-20

On-Brand Devices [BD Introsyte-N, BD Instaflash]

• 50382903840217: INTRODUCER INTROSYTE-N 1.9F 1.9CM
• 00382903840212: INTRODUCER INTROSYTE-N 1.9F 1.9CM