BD Introsyte Autoguard 384011

GUDID 00382903840113

INTROSYTE AUTOGUARD 18G INTRO ONLY

BECTON, DICKINSON AND COMPANY

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• Primary Device ID: 00382903840113
• NIH Device Record Key: 1b4951ee-27b6-4172-b571-bab8e9a649a3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Introsyte Autoguard
• Version Model Number: 384011
• Catalog Number: 384011
• 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	00382903840113 [Primary]
GS1	50382903840118 [Package]; Package: Case [10 Units]; In Commercial Distribution

FDA Product Code

• DYB: Introducer, catheter

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2024-03-11
• 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