BD Intelliport System 516800

GUDID 00382905168000

SYRINGE LABELER

BECTON, DICKINSON AND COMPANY

Intravenous injection automated detection/documentation system processor/transmitter

• Primary Device ID: 00382905168000
• NIH Device Record Key: 98c5e125-3574-4431-ad7d-5240df32a762
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Intelliport System
• Version Model Number: 516800
• Catalog Number: 516800
• Company DUNS: 001292192
• Company Name: BECTON, DICKINSON AND COMPANY
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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	00382905168000 [Primary]

FDA Product Code

• PCH: Gastrointestinal pathogen panel multiplex nucleic acid-based assay system

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-06-17
• Device Publish Date: 2024-06-07

On-Brand Devices [BD Intelliport System]

• 60382905168033: SYRINGE LABELER INK CARTRIDGE
• 60382905168026: SYRINGE LABELER BARREL LABEL ROLL
• 50382905168012: SYRINGE LABELER LUER LABEL CASSETTE
• 00382905168000: SYRINGE LABELER