BD Introsyte Autoguard 384010

GUDID 50382903840101

INTROSYTE AUTOGUARD 20G INTRO ONLY

BECTON, DICKINSON AND COMPANY

Vascular catheter introduction set, nonimplantable

• Primary Device ID: 50382903840101
• NIH Device Record Key: bcecb5ae-bc55-4f60-8793-b3586d4feb1a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Introsyte Autoguard
• Version Model Number: 384010
• Catalog Number: 384010
• 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	00382903840106 [Unit of Use]
GS1	50382903840101 [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 Autoguard]

• 50382903840125: INTROSYTE AUTOGUARD 16G INTRO ONLY
• 50382903840118: INTROSYTE AUTOGUARD 18G INTRO ONLY
• 50382903840101: INTROSYTE AUTOGUARD 20G INTRO ONLY
• 00382903840113: INTROSYTE AUTOGUARD 18G INTRO ONLY
• 00382903840106: INTROSYTE AUTOGUARD 20G INTRO ONLY
• 00382903840120: INTROSYTE AUTOGUARD 16G INTRO ONLY