BD Intelliport 516706

GUDID 60382905167067

KIT GATEWAY

BECTON, DICKINSON AND COMPANY

Anaesthesia information system application software Anaesthesia information system application software Anaesthesia information system application software Anaesthesia information system application software Anaesthesia information system application software Anaesthesia information system application software Anaesthesia information system application software Anaesthesia information system application software Anaesthesia information system application software Anaesthesia information system application software Anaesthesia information system application software Anaesthesia information system application software Anaesthesia information system application software Anaesthesia information system application software

• Primary Device ID: 60382905167067
• NIH Device Record Key: d7c3aa71-61e7-4c2b-9c03-7d6dcba011b5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Intelliport
• Version Model Number: 516706
• Catalog Number: 516706
• 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	00382905167065 [Primary]
GS1	60382905167067 [Package]; Contains: 00382905167065; 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