BD Intelliport 516750

GUDID 60382905167500

MOUNT

BECTON, DICKINSON AND COMPANY

Intravenous injection automated detection/documentation system processor/transmitter Intravenous injection automated detection/documentation system processor/transmitter Intravenous injection automated detection/documentation system processor/transmitter Intravenous injection automated detection/documentation system processor/transmitter Intravenous injection automated detection/documentation system processor/transmitter Intravenous injection automated detection/documentation system processor/transmitter Intravenous injection automated detection/documentation system processor/transmitter Intravenous injection automated detection/documentation system processor/transmitter Intravenous injection automated detection/documentation system processor/transmitter Intravenous injection automated detection/documentation system processor/transmitter Intravenous injection automated detection/documentation system processor/transmitter Intravenous injection automated detection/documentation system processor/transmitter Intravenous injection automated detection/documentation system processor/transmitter Intravenous injection automated detection/documentation system processor/transmitter

• Primary Device ID: 60382905167500
• NIH Device Record Key: 8d4bb67d-e278-4514-93e7-0539fe2de25e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Intelliport
• Version Model Number: 516750
• Catalog Number: 516750
• 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

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature

Device Identifiers

Device Issuing Agency	Device ID
GS1	00382905167508 [Primary]
GS1	60382905167500 [Package]; Contains: 00382905167508; Package: Carton [10 Units]; In Commercial Distribution

FDA Product Code

• PHC: Infusion safety management software

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: 2020-10-08
• Device Publish Date: 2020-09-30

On-Brand Devices [BD Intelliport]

• 60382905167012: BASE
• 00382905167003: SENSOR
• 60382905167500: MOUNT
• 60382905167067: KIT GATEWAY
• 00382905167041: KIT TABLET