CARDIOTOMY RESERVOIR

GUDID 38033178250376

SORIN GROUP ITALIA SRL

Cardiotomy reservoir

• Primary Device ID: 38033178250376
• NIH Device Record Key: 391509d7-3103-4561-81a9-e22f0cfb3fc4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CARDIOTOMY RESERVOIR
• Version Model Number: FILTERED
• 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	08033178250375 [Primary]
GS1	38033178250376 [Package]; Contains: 08033178250375; Package: BOX [6 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K902437

FDA Product Code

• DTP: Defoamer, 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: 2020-01-22
• Device Publish Date: 2015-07-15

On-Brand Devices [CARDIOTOMY RESERVOIR]

• 38033178250376: FILTERED
• 38033178109674: UNFILTERED