BD Introsyte-N 384031

GUDID 00382903840311

INTRODUCER INTROSYTE-N 2.8F 2.5CM

BECTON, DICKINSON AND COMPANY

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• Primary Device ID: 00382903840311
• NIH Device Record Key: 10ba20ef-4c12-4c3a-bc59-44f94334dd07
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Introsyte-N
• Version Model Number: 384031
• Catalog Number: 384031
• Company DUNS: 124987988
• Company Name: BECTON, DICKINSON AND COMPANY
• Device Count: 1
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00382903840311 [Primary]
GS1	50382903840316 [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-N]

• 50382903840316: INTRODUCER INTROSYTE-N 2.8F 2.5CM
• 00382903840311: INTRODUCER INTROSYTE-N 2.8F 2.5CM