Paediatric Venous Cannula

GUDID 38033178004535

SORIN GROUP ITALIA SRL

Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, venous

• Primary Device ID: 38033178004535
• NIH Device Record Key: 38ee0682-714e-4086-ac89-b047a8840c0b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Paediatric Venous Cannula
• Version Model Number: V132-12
• Company DUNS: 442126587
• Company Name: SORIN GROUP ITALIA SRL
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08033178004534 [Primary]
GS1	38033178004535 [Package]; Contains: 08033178004534; Package: BOX [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K890980

FDA Product Code

• DWF: CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2022-08-05
• Device Publish Date: 2016-03-21

On-Brand Devices [Paediatric Venous Cannula]

• 38033178004573: V132-20
• 38033178004566: V132-18
• 38033178004559: V132-16
• 38033178004542: V132-14
• 38033178004535: V132-12
• 38033178004528: V132-10