High Pressure Hose and Yoke 710603

GUDID 30815112021291

High Pressure Hose and Yoke

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: 30815112021291
• NIH Device Record Key: ee4b6ec0-f1c4-4899-b60e-939018eb61a1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: High Pressure Hose and Yoke
• Version Model Number: 710603
• Catalog Number: 710603
• 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: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• 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	30815112021291 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K030854

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 [High Pressure Hose and Yoke]

• 30815112020799: High Pressure Hose and Yoke
• 30815112021291: High Pressure Hose and Yoke