Suction tip

GUDID 38033178018754

SORIN GROUP ITALIA SRL

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• Primary Device ID: 38033178018754
• NIH Device Record Key: 62c9fbea-e07c-4ef2-9110-8ebe0018ff00
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Suction tip
• Version Model Number: SU-29602
• Company DUNS: 442126587
• Company Name: SORIN GROUP ITALIA SRL
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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	08033178018753 [Primary]
GS1	38033178018754 [Package]; Contains: 08033178018753; Package: BOX [10 Units]; In Commercial Distribution

FDA Product Code

• DTS: Sucker, cardiotomy return, cardiopulmonary bypass

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-03-28
• Device Publish Date: 2024-03-20

On-Brand Devices [Suction tip]

• 38033178018754: SU-29602
• 38033178018747: SU-26702
• 38033178018730: SU-22702
• 38033178018723: SU-20802
• 38033178018716: SU-20602
• 38033178018709: SU-20601
• 38033178018679: SU-12502
• 38033178018662: SU-12402
• 38033178018655: SU-12202
• 38033178018648: SU-10101