Protocol Touch Colon Insufflator 390308

GUDID 30815112021239

Protocol Touch Colon Insufflator

BRACCO DIAGNOSTICS INC

Gastrointestinal endoscopic insufflator Gastrointestinal endoscopic insufflator Gastrointestinal endoscopic insufflator Gastrointestinal endoscopic insufflator Gastrointestinal endoscopic insufflator Gastrointestinal endoscopic insufflator Gastrointestinal endoscopic insufflator Gastrointestinal endoscopic insufflator Gastrointestinal endoscopic insufflator Gastrointestinal endoscopic insufflator Gastrointestinal endoscopic insufflator Gastrointestinal endoscopic insufflator Gastrointestinal endoscopic insufflator Gastrointestinal endoscopic insufflator Gastrointestinal endoscopic insufflator

• Primary Device ID: 30815112021239
• NIH Device Record Key: f078864c-530c-419a-9fcd-2cd337c7aebf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Protocol Touch Colon Insufflator
• Version Model Number: 390308
• Catalog Number: 390308
• Company DUNS: 849234661
• Company Name: BRACCO DIAGNOSTICS INC
• 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: 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 609-514-2200
• Email: xx@xx.xx
• Phone: 609-514-2200
• Email: xx@xx.xx
• Phone: 609-514-2200
• Email: xx@xx.xx
• Phone: 609-514-2200
• Email: xx@xx.xx
• Phone: 609-514-2200
• Email: xx@xx.xx
• Phone: 609-514-2200
• Email: xx@xx.xx
• Phone: 609-514-2200
• Email: xx@xx.xx
• Phone: 609-514-2200
• Email: xx@xx.xx
• Phone: 609-514-2200
• Email: xx@xx.xx
• Phone: 609-514-2200
• Email: xx@xx.xx
• Phone: 609-514-2200
• Email: xx@xx.xx
• Phone: 609-514-2200
• Email: xx@xx.xx
• Phone: 609-514-2200
• Email: xx@xx.xx
• Phone: 609-514-2200
• Email: xx@xx.xx
• Phone: 609-514-2200
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10815112021235 [Primary]
GS1	30815112021239 [Package]; Contains: 10815112021235; Package: Box [1 Units]; In Commercial Distribution

FDA Product Code

• FCX: Insufflator, Automatic Carbon-Dioxide For Endoscope

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: 2023-09-08
• Device Publish Date: 2023-08-31

On-Brand Devices [Protocol Touch Colon Insufflator]

• 10815112020672: Protocol Touch Insufflator
• 30815112021239: Protocol Touch Colon Insufflator