Injector Head

GUDID 37630039300891

Bracco Injeneering SA

CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary CT contrast medium injection system, line-powered, stationary

• Primary Device ID: 37630039300891
• NIH Device Record Key: aa90bee4-c729-4f0b-8455-e96ddbb52653
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Injector Head
• Version Model Number: 102410
• Company DUNS: 482489007
• Company Name: Bracco Injeneering SA
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment
• Special Storage Condition, Specify: Between 0 and 0 *Dry environment

Device Identifiers

Device Issuing Agency	Device ID
GS1	17630039300910 [Primary]
GS1	37630039300891 [Package]; Contains: 17630039300910; Package: box [1 Units]; In Commercial Distribution

FDA Product Code

• JAK: System, X-Ray, Tomography, Computed

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: 2021-03-15
• Device Publish Date: 2021-03-05

On-Brand Devices [Injector Head]

• 37630039300396: 017377
• 37630039301041: 102410
• 37630039300891: 102410
• 17630039302037: 102410
• 17630039301962: 102410